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Dr.

Konrad Werthmann

Isopathic/Homeopathic Materia Medica

Edition 2005

Disclaimer:
The purpose of this book is to provide information about the use of the SANUM preparations for a wide range of medical problems only. However, illness can be highly unpredictable, and therefore, one should seek the best possible medical expertise. No liability is accepted by the author and/or the publishers for any claims arising from the administration, prescribing strategy or use of any of the remedies described.

To the Reader:
This Isopathic/Homeopathic Materia Medica of Sanum medicinal products has been compiled from research conducted by leading homeopathic practitioners in and outside of Germany. The collected research and uses discussed in the Materia Medica have been reviewed by a distinguished panel. This valuable compilation of known medicinal uses of the Isopathic/Homeopathic remedies is made available to interested practitioners and researchers in many countries. The production process of the homeopathics covered by this Materia Medica is strictly based on the German Homeopathic Pharmacopoeia (Homopathisches Arzneimittelbuch), which essentially has been adopted by many other countries. However, because not all products, dosage forms or intended uses are available or approved by the relevant authorities in all national markets, practitioners are advised to seek local guidance regarding the legal status of the products and intended uses in their areas. For example, the oral portable SIPS (1 and 2 ml vials) are at this time available only in the United States of America. Our thanks to all those who have made publication of this Materia Medica possible and to the peer reviewers and practitioners who have contributed their time and effort to disseminate this information.

Published by Semmelweis-Institut Verlag fr Naturheilkunde GmbH D - 27316 Hoya. Copyright by Semmelweis-Institut All rights reserved, including those of translations into foreign languages. It is not permitted to reproduce any part of this book in any form, copying, printing, microfilming or scanning or audio taping without written permission of the publisher. Alle Rechte vorbehalten, insbesondere die der bersetzung in fremde Sprachen. Dieses Buch oder Teile dieses Buches drfen ohne schriftliche Genehmigung des Verlages in keiner Form - durch Fotokopie, Mikrofilm oder irgend einem anderen Verfahren - reproduziert werden oder in eine von Maschinen verwendbare Sprache bersetzt oder bertragen werden. Tous droits rservs, particulirement ces de traduire en une langue trangre. Sans autorisation par crit du diteur il est interdit de reproduire ce livre ou parts de ce livre en aucune forme - par photocopie, microfilm ou une autre mthode - ou de le traduire en une langue qui peut tre utiliser par des machines. Reservado todos los derechos, especialmente los de la traduccin a idiomas extranjeros. Sin autorizacin escrita del editor original, este libro no puede reproducirse ni parcial ni totalmente, en cualquier forma que sea, electrnica o mecnica; mediante fotocopia, mimegrafo o cualquier sistema de grabacin en disco o cinta de ordenador. Edition 2005 Printed in Germany by Druckerei Adam Prettenhofer GmbH & Co. KG

Contents
Preface Scheme for a Basic Therapy of Chronic Diseases SANUM Elimination Cure Albicansan (fungal preparation) Alkala N (mineral & trace elements) Arthrokehlan A (bacterial Arthrokehlan U (bacterial
preparation) preparation)

8 23 23 Drops 5X, Amps. 5X, Caps. 4X, Supps. 3X, Ointment 3X Powder Drops 6X, Amps. 6X Drops 6X, Amps. 6X Drops 6X, Amps. 6X, Caps. 5X, Supps. 5X Drops 3X, Tabs. 4X Drops 1X, Amps. 3X Amps. 3X, 5X Drops 10X/30X/200X, Amps. 10X/30X/200X, Tabs. 10X/30X/200X Drops 3X, Amps. 4X Drops 1X Drops 5X, Amps. 5X, Supps. 3X Drops 5X, Amps. 5X Drops 6X/12X/30X/200X, Amps. 6X/12X/30X/200X Drops 5X, Amps. 5X, 6X Tabs. 5X, Caps. 4X, Supps. 3X Drops 1X, 4X, Amps. 4X Drops 5X, Amps. 5X Drops Drops 5X, Amps. 5X, Caps. 4X, Supps. 4X Drops 6X, Amps. 4X, 6X; Caps. 4X, 6X; Supps. 6X Drops 1X 24 29 30 33 36 41 43 45 47 53 57 59 62 64

Bovisan (bacterial preparation) Calvakehl (fungal preparation) Cerivikehl (herbal preparation) Chrysocor (organ preparation) Citrokehl (citric acid) Cuprukehl (copper gluconate) Episcorit (herbal preparation) Exmykehl (fungal preparation) Fomepikehl (fungal preparation) Formasan (formic acid)

Fortakehl (fungal preparation) Ginkgobakehl (herbal preparation) Grifokehl (fungal preparation) Hexacyl (herbal & mineral preparation) Larifikehl (fungal preparation) Latensin (bacterial preparation)

67 79 82 84 86 90

Leptospermusan (herbal preparation)

98

Leptucin (bacterial preparation) Lipiscor (polyunsaturated fatty acids) Luffasan (herbal preparation) Mapurit (vitamin and mineral) Mucedokehl (fungal preparation) Mucokehl (fungal preparation) Mucokehl Atox (Excretion) Muscarsan (fungal preparation) Nigersan (fungal preparation)

Caps. 6X, Supps. 6X Caps. Drops 4X, Tabs. 4X Caps. Drops 5X, Amps. 5X, Caps. 4X, Supps. 3X

99 101 103 105 107

Drops 5X, Amps. 5X, 6X, 7X; Tabs. 5X, 111 Caps. 4X, Supps. 3X, Ointment 3X, Eye Drops 5X Drops 6X, Amps. 6X Drops 6X, Amps. 4X, Tabs. 6X Drops 5X, Amps. 5X, 6X, 7X; Tabs. 5X, Caps. 4X, Supps. 3X Drops 6X, Amps. 6X Drops 5X, Amps. 5X, 6X, 7X; Tabs. 5X, Caps. 4X, Supps. 3X, Ointment 3X Drops 2X, Tabs. 2X Drops 5X, Amps. 6X, Caps. 4X, Supps. 3X, Ointment 3X Drops 5X, Amps. 5X, Caps. 4X, Supps. 4X Drops 2X Drops 9X Drops 9X Drops 9X Drops 9X Drops 9X Drops 9X Drops 9X Drops 9X Drops 9X Drops 9X Drops 5X, Amps. 5X, Caps. 4X, Supps. 3X 129 131 137

Nigersan Atox (Excretion) Notakehl (fungal preparation)

151 153

Okoubasan (herbal preparation) Pefrakehl


(fungal preparation)

169 171

Pinikehl (fungal preparation) Pleo Chelate Polysan A (in vitro diagnosticum) Polysan D (in vitro diagnosticum) Polysan Dx (in vitro diagnosticum) Polysan E (in vitro diagnosticum) Polysan G (in vitro diagnosticum) Polysan K (in vitro diagnosticum) Polysan M (in vitro diagnosticum) Polysan Om (in vitro diagnosticum) Polysan R (in vitro diagnosticum) Polysan T (in vitro diagnosticum) Quentakehl (fungal preparation)

181 185 187 189 191 193 195 197 199 201 203 205 207

Rebas (organ preparation) Recarcin (bacterial preparation) Relivora Complex (herbal preparation) Ruberkehl (fungal preparation) Sankombi (fungal preparation) Sanoryzae (fungal preparation) Sanukehl Acne (bacterial preparation: haptens)

Amps. 4X, 12X; Caps. 4X, 6X; Supps. 4X, 6X

215

Drops 6X, Amps. 4X, 6X; Caps. 4X, 6X; Supps. 6X 227 Drops 2X/3X/4X, Amps. 3X/4X/4X Drops 5X, Amps. 5X, Supps. 3X Drops 5X Drops 6X Drops 6X, Amps. 5X 239 243 246 248 249 252 255 259 262 265 269 273 276 279 282 285 288 291 292

Sanukehl Brucel (bacterial preparation: haptens) Drops 6X, Amps. 6X Sanukehl Cand (fungal preparation: haptens) Sanukehl Coli (bacterial preparation: haptens) Drops 6X, Amps. 5X Drops 6X, Amps. 7X

Sanukehl Klebs (bacterial preparation: haptens) Drops 6X, Amps. 6X Sanukehl Myc (bacterial preparation: haptens) Sanukehl Prot (bacterial preparation: haptens) Sanukehl Pseu (bacterial preparation: haptens) Drops 6X, Amps. 5X Drops 6X, Amps. 7X Drops 6X, Amps. 5X

Sanukehl Salm (bacterial preparation: haptens) Drops 6X, Amps. 6X Sanukehl Serra (bacterial preparation: haptens) Drops 6X, Amps. 5X Sanukehl Staph (bacterial preparation: haptens) Drops 6X, Amps. 5X Sanukehl Strep (bacterial preparation: haptens) Drops 6X, Amps. 5X Sanukehl Trich (fungal preparation: haptens) Sanumgerman
(di-potassium-germanium(IV)-citrate-L(+)lactate)

Drops 6X, Amps. 5X Drops 6X Drops 4X/6X/12X/30X/200X, Amps. 4X/6X/12X/ 30X/200X, Tabs. 4X/6X/12X/ 30X/200X, Ointment 1X Drops 4X, Amps. 4X Caps. Drops 6X

Sanuvis (lactic acid)

Selenokehl (sodium selenite) Silvaysan (herbal preparation) Stolonikehl (fungal preparation)

300 304 306 307 310 316

Strophanthus 4X Sanum (herbal preparation) Drops 4X, Tabs. 4X Thymokehl (organ preparation) Usneabasan (herbal preparation) Amps. 6X, Caps. 6X, Supps. 6X Drops 1X

Ustilakehl (fungal preparation) Utilin (bacterial preparation) Utilin S (bacterial preparation) Vitamin B Komplex Sanum N (vitamins) Vitamin E Sanum (vitamins) Zinkokehl (zinc gluconate) Disease List

Drops 5X, Amps. 5X, Supps. 5X Drops 6X, Amps. 4X, 6X; Caps. 4X, 6X; Supps. 6X Drops 6X, Amps. 4X, 6X; Caps. 4X, 6X; Supps. 6X Amps. Amps. Drops 3X, Amps. 4X

317 321 333 341 343 345 347

Preface
Origins of Pleomorphism
The concepts of pleomorphism and symbiosis are in the current perspective inseparable from the name of the great researcher and microbiologist, Professor Dr. Gnther Enderlein (1872-1968). The basis for his work was the book by the French researcher A. Bchamp, titled Microzymas. It described that a microorganism can, under precisely determined preconditions, occur in diverse developmental stages and, especially also in diversified forms, without the loss of its specific characteristics. The microorganism may vary from the smallest rungs of electron microscopic magnitude up to the large, multinucleic and highly developed stages, such as of bacteria and fungi. Moreover, Bchamp was able to prove that all animal and plant cells contain tiny particles which continue to live after the death of the organism and out of which microorganisms can develop. In this book, Bchamp laid the foundation for the concept of pleomorphism. The view that microorganisms can undergo a considerable variation in form, without losing their specific functions, stood and continues to stand diametrically opposed to the prevailing opinion of monomorphism, which admits only a single form and function to an organism. Naturally, that opinion has also resulted in a monomorphistic view of every disease process. Thus, in contrast to the opinion of Pasteur, that microorganisms simply exist without any developmental changes, Enderlein through intensive research came to the conclusion that the monomorphistic perspective of disease processes can no longer be maintained and had to be given up in favor of a pleomorphic perspective. He proved that every organism houses a primal plant germ in erythrocytes, which can very well become subject of a variation in form through exogenic influences.

Pleomorphism and Cyclogeny


The opinion represented by pleomorphic bacteriologists of the fundamental changeability of forms holds the possibility for microorganisms to abruptly change from originally avirulent into potentially virulent conditions. Enderlein devoted the bulk of his scientific work which stretched for more than 40 years, to the complex question of pleomorphism, symbiosis and cyclogeny of microorganisms. He published over 500 scientific articles. His chief work was titled Bacteria Cyclogeny, Berlin, 1925. In this book he described in detail the changes and development of the parasite in its variable forms and its cycle. It is currently published by Semmelweis Verlag, Hoya, in the German language; it is available in English language from Pleomorphic Product Sales Inc., Glendale, AZ, USA. This research was initiated by Enderlein in the year 1916, while he was working on typhoid. In blood using a darkfield microscope he observed mobile, tiniest

living forms, named Spermits, which copulated with higher organized structures, whereafter the product of the copulation became suddenly invisible. Enderlein interpreted this as sexual processes, whereby tiniest, final products occurred, which are not visible to the eye of the light microscope. He named the symbiotic, primal plant germ in the erythrocyte Endobiont. This Endobiont lives in genuine symbiosis with the host organism, that is, with mutual benefits. Through outer factors, the Endobiont can multiply and develop - a process which can considerably disturb the symbiotic equilibrium. A healthy organism is capable of restoring the equilibrium. In this process, the more highly developed pathogenic germs are broken down into avirulent primitive forms through the copulation described by Enderlein. They leave the body through the natural organs of elimination.

The Nature of the Primal Germs and Symbiosis


However, the capacity for regenerating symbiosis is usually massively weakened through unhealthy lifestyles that are not in harmony with nature! Symbiosis is completed when the symbiont makes itself independent and becomes a parasite. In this, the Endobiont undergoes three basic phases: colloid-bacterium-fungus. This means, it develops from the apathogenic, non-mobile, tiniest albuminoid particle (Protit) - which is to be classified in size with the viruses (0.01 m) - via the nonvirulent chondrit stage into the parasitic, pathogenic stages such as bacterium and fungus. According to Enderlein, they are not representing unchanging organisms that are independent of each other, but altogether they form a singular, common cycle, which has its origin in the colloidal, albuminoid substances that are contained inside of each particular cell.

Diseases of the Endobiosis Complex


Assisted by darkfield microscopy and using living blood, Enderlein was able to deliver clear proof of this vital, microbiological process in both its origin and cycle. As soon as this vital happening leaves a defined condition of equilibrium, all signs of parasitism occur, whereby out of the apathogenic symbionts (Protits and Chondrits) - with their enzymatic and metabolic active properties, they develop pathogenic microorganisms. This explains, according to Enderlein, that all diseases of the Endobiosis complex are based on the upward development of the Endobiont into higher valenced, parasitic growth forms with their own metabolism that is harmful for body fluids. These disease processes are difficult to fathom, as they make themselves known in the beginning by functional disorders in most diversified organs, such as, by headaches, high or low blood pressure, feeling poorly, unmotivated attitude, lack of appetite, drab complexion, coated tongue, wounds in the mouth, pimples, sores, hoarseness, catarrhs, ear noises, diarrhea, lowered capacity for seeing and hearing, depressions, weak concentration or poor memory. Diseases, however, also indicate healing processes, which attempt to return a disturbed symbiosis to the original healthy condition. Whether the biological self-healing forces of the organism will win over the disease, or whether the

symbiont is able to develop unchecked into a parasite, depends on the condition of the milieu in which the disturbance plays out. If the inner milieu is damaged through unhealthy nutrition and lifestyles, with their resultant disturbance of the acid-base equilibrium, through environmental toxins, through constant infections, or even through psychological depressions, then our self-healing forces are incapable of restoring our symbiotic equilibrium. Disease will manifest and damage the body. According to Enderlein, the milieu-conditioned cyclogenetic rise into higher stages of those microorganisms developed from the symbiont always determine the disease.

Foundations for Isopathic Therapy


Enderlein developed Isopathic Therapy with its specific biological remedies for all nonspecific, general symptoms that pertain to the Endobiosis Complex, based on the knowledge of the mutability of forms and the fact of the biological, and essential for life symbiosis between the mammal organism and the Endobiont. This unique perspective, at that time, distinguishes Enderlein as a pioneer of a modern, ecological world-view and puts monomorphism, which is still being taught, in question. In his Bacteria Cyclogeny, Enderlein describes the development of the two mold fungi species Aspergillus niger van Tieghem (SA 4-20) and Mucor racemosus Fresen (SA 4-11), beginning from the primitive phases as tiniest colloidal albuminoid particles, via the bacterial phase, up to the fungal stage. Both fungal species, which are likely obtained transplacentally, can occur as Endobionts in all their developmental stages within mammal bodies. Although their occurrence may be more or less frequent, they are to be seen as the cause of numerous ailments. The tubercular and paratubercular diseases, caused by pathogenic Aspergillus stages, do not occur quite as frequently as the disease processes more frequently caused by pathogenic Mucor phases arising from the Mucor symbiosis. The presence of the Endobiont in mammal organisms has been termed Endobiosis by Enderlein since 1946. By this are meant the apathogenic, low valanced phases of the Mucor racemosus Fresen (SA 4-11) (Protits, Symprotits, Chondrits, Fibrin). Fibrin is the highest developmental form of the Chondrit, before the Endobiont changes from the primitive phase into the bacterial phase (analogously to Siphonospora polymorpha v. Brehmer). In these lower valences, the symbiont supports the metabolism of the host organism, thus strengthening the defense. The higher the Endobiont rises in its developmental series, the more it increases in toxicity. The upward development of the Endobiont via the Chondrit form and higher is the cause for the endobiontic diseases, up to the death of the host organism. In the course of this process, the Endobiont is most likely partaking in the development of tumors. In the stages of precancerosis, one finds higher valenced Endobionts in the blood. According to Devrient, the cancer problem cannot be solved without regard to blood parasitism and polymorphism of the microorganisms. For Enderlein, cancer is for the

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host organism a fermentation and decomposition condition, forced upon it by a parasitic fungus and its developmental forms. Because the Endobiont devours protein greedily, its upward development and the Endobiosis or congestion resulting from it are especially co-created through improper nutrition. Among these diseases belong vascular changes, pathological coagulatory processes, geloses, rheumatism, arthritis, spondylosis, tonsillitis, lymphogranulomatosis, diabetes, gout, tumors of every type (even those that are benign and their prestages), anemia, leukemia, cerebral sclerosis and paralyses. The restriction of protein intake causes the return to lower phases, which then leave the body via the organs of excretion.

The Isopathic Preparations of the Fungal Phase


Another possibility for the breakdown of higher forms into lower stages is the exogenous supply of the so-called Chondritins in the quoted isopathic therapy. According to Enderlein, Chondritins are apathogenic, low developmental stages of diverse fungi, which can be either of a specific nature, as in the Mucor racemosus Fresen (SA 4-11) and Aspergillus niger von Tieghem (SA 4-20), or of an unspecific nature such as in Penicillium chrysogenum (SA 4-30) and Penicillium glabrum (SA 4-31). The specific Chondritins metabolize the virulent, parasitic microorganisms by copulation, thereby initiating their breakdown. The nonspecific Chondritins act as stimulating irritants by supporting the defensive capacity of the human organism through absorbing the ferments of foreign microbes. Chondritins from diverse mold fungi and yeasts are available for application, for example, in the following preparations (see Table of Contents): ALBICANSAN, Candida albicans EXMYKEHL, Candida albicans, Candida parapsilosis, Penicillium roquefortii FOMEPIKEHL, Fomitopsis pinicola FORTAKEHL, Penicillium roquefortii LARIFIKEHL, Laricifomes officinalis MUCEDOKEHL, Mucor mucedo MUCOKEHL, Mucor racemosus NIGERSAN, Aspergillus niger NOTAKEHL, Penicillium chrysogenum PEFRAKEHL, Candida parapsilosis PINIKEHL, Fomitopsis pinicola QUENTAKEHL, Penicillium glabrum RUBERKEHL, Aspergillus ruber SANKOMBI, Mucor racemosus, Aspergillus niger SANORYZAE, Aspergillus oryzae STOLONIKEHL, Penicillium brevicompactum (formerly: Penicillium stoloniferum) These remedies have been developed partly by Enderlein himself and partly on the basis of his most valuable research. They act in the way of isopathy; that means, they are not directed against the disease or its symptoms, but they support

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the bodys own capabilities for regeneration, whereby genuine healing processes become possible. Isopathic Therapy nonviolently normalizes the symbiontic equilibrium between the Endobiont and its host organism on a basis of speciesidentical organisms. In addition, through the administration of the so-called anti-Chondritins MUCOKEHL Atox (Excretion) and NIGERSAN Atox (Excretion), antibodies for the fungal Chondritins, both their breakdown and their elimination through the urinary paths, the bronchi, the skin, and especially the intestine, can be accelerated. The preparations FOMEPIKEHL, LARIFIKEHL, PINIKEHL, RUBERKEHL, SANORYZAE and STOLONIKEHL represent fungal preparations, which have had traditional healing reputations in folk medicine; these preparations are produced as isopathic substances based on the knowledge of Prof. Dr. Enderlein.

The Therapy of Candidiasis with Isopathic Preparations


ALBICANSAN holds a special position among the isopathic preparations. This preparation contains Chondritins of Candida albicans in diverse homeopathic dilutions as its active substance. The therapeutic principle of the Candida preparations is based on the dimorphism of the yeast organism, sometimes also referred to as Soorpilz. The organism may exist in several growth forms or developmental phases, as yeast and as fungus. Consequently, it is living proof for the accuracy of Enderleins Theory of Pleomorphism. In its yeast form, the organism exists as a single cell. Candida yeasts are saprophytic, which become pathogenic only under certain preconditions. A weakened immune system, or antibiotic treatment, promotes the pathogenicity of Candida yeast cells enormously. They are the cause for the far-spreading Candidiasis in the form of a superficial colonization on mucous membranes. If the infested host cell dies, the yeast cell comes into contact with dissolving cell fragments and the cell fluid. This is the signal for the yeast cell to rise within the cyclogenetic series into a parasitic, mycelia forming fungus, which then grows invasively into the tissues and, thereby, initiates the widening of tissue lesions. The preparation ALBICANSAN takes this dimorphism (the varying between yeast and fungus) into account in the therapy. Researchers have succeeded in cultivating the microorganism as yeast phase and also as fungal phase, side by side, through appropriate conditions of cultivation. Therefore, the superficial mucous membrane associated forms of Candidiasis, the deeper settled, tissue infiltrating infections, and also massive intestinal mucosal forms can become therapeutic. Moreover, the well-proven preparation PEFRAKEHL is available for Candidiasis therapy. It can also be applied, among other possibilities, as a cross antigen reaction that is effective for superficial Candida albicans infections. PEFRAKEHL is a preparation from the yeast form of Candida parapsilosis, which is predominantly isolated from the skin, from nail bed infections, Otitis externa and Endo-

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carditis in human beings; a most effective preparation. A must for every practice! EXMYKEHL represents a combination of Candida albicans, Candida parapsilosis and Penicillium roquefortii.

General Comments on Isopathic Preparations


In the application of isopathic preparations, the guiding rule is that an increase in the dosage may be undertaken only when the previous or identical dosages no longer bring effective action. Every overdose has an excessive production of toxic decomposition forms as its consequence. The task of the tissues in removing these decomposition products out of the body, namely through the skin, the intestine, the urinary passages and the bronchi - can, then, only be insufficiently or not at all fulfilled. In the case of massive disease foci, such a condition can occur even with greatest precaution, and it can bring the healing processes to a slower pace or even stop them. By repeated injection of detoxified active fungal antibodies (Anti-Chondritins), the elimination of each form of decomposition is accelerated and, thereby, the effectiveness of the isopathic preparation becomes enhanced. The darkfield examination of the blood reveals such toxic conditions, caused by the congestion of endobiontic decomposition products. At such times there is a fundamental need to look well to the effective functioning of the organs of elimination (stool, urine, sweat, sputum). Under circumstances, a detoxification therapy (enemas, baths, teas, electrolytes) may be required. The decomposition products of the Endobiont that are eliminated on an ongoing basis without treatment under healthy conditions may, in patients, again adopt higher valences or higher developmental stages during their outward passage through the skin, intestine, urinary paths and bronchi. This way, especially in cancer cases, short rods frequently form in the intestines. Because they are shaped like coli bacteria, they are easily misinterpreted as degenerated coli bacteria. These forms are usually easily decomposed within twelve hours after administration of the relevant capsule form, which decompose them again into the Chondrit stage. These forms, which are also referred to as Paracoli, cause intense constipation and must be closely watched in cancer cases. For this reason, Isopathic Therapy plays an important role also in the treatment of constipation and dysbacteria. Because MUCOKEHL (Mucor racemosus) also effects decongestion of agglutinated erythrocytes, leucocytes, thrombocytes, etc., an appropriate massage of connective tissues and muscles is of especially supportive significance. The myogeloses, painful points, etc. affected thereby are nothing but the accumulation of low-valanced developmental stages. Every isopathic treatment can be performed with oral, inhalable, or percutaneously rubbed-in preparations, suppositories, or through injection. These diverse forms of application can be combined or alternatively administered, according to the situation of the case. The intake, inhalation and rubbing are milder in effect and suitable for prophylactic treatment during the intervals that are free

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from injections, and for follow-up treatments. Drops are also very effective when dropping 1-2 drops into each nostril.

Application as injections
In general, one begins an injection series with the weakest strength (for example 7X). In case of no reaction, one changes to 6X and finally to 5X.

Application of the Fungal Antibodies


Fungal antibodies (Antichondritins) serve for freeing the blood of stronger infestation by decomposition products of the Endobiont after Chondritin injections. These do not affect the higher cyclic forms, such as bacteria, but only the decomposition products in the primitive phases. On the first or second day after administering injections, 1 ml is injected s.c. or i.m.; this can be repeated in identical intervals.

External Application
Percutaneous application, according to the style of the Ponndorf Inoculation or the Baunscheidt Method, raises the effectiveness of the isopathic remedy. In the area of the diseased organ, or else in the elbow bends or groin, 5-10 drops daily, or at longer intervals, externally rubbed in on injection-free days. Eye drops are dropped into the palpebral tissue. The ointment is applied on the affected skin portions 1-3 times daily.

Application as an Inhalation
Using a sterile pocket inhalator, the drop form is externally inhaled; 10-20 drops inhaled deeply, 2-3 times daily through the mouth and nose. The inhalator must not contain even a trace of any cleaning agent!

Internal Application
The oral fungus preparations support the effect of the injected, rubbed in and inhaled preparations; they have, moreover, a local impact on disease processes, especially in the gastrointestinal canal. Tablets or capsules can be taken with or without food. One swallows the capsules with a little water. The tablets should be allowed to melt under the tongue. The appropriate combination of preparations from the endobiontic series is definitely possible and useful. However, NOTAKEHL (Penicillium chrysogenum) must not be taken simultaneously with MUCOKEHL (Mucor racemosus) or SANKOMBI (Mucor racemosus/Aspergillus niger) because these preparations weaken or nullify their effects mutually (antagonism).

Additional Measures
The normalization of the blood pH must be given very special significance in all diseases of the Endobiosis complex. This is especially required if the patients blood shows a Protit veil after a Chondritin injection, because it always points to a raised pH or rH2 value of the blood. The stress that is thereby exerted on the circulation of the blood aggravates or blocks the desired copulation of the

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Chondrits. An injection of L(+) lactic acid (SANUVIS) several minutes before the Chondritin injection is recommended for the necessary adjustment of the pH value. In regard to additional biological therapy in general, the therapist naturally remains in control of all possibilities during the period of isopathic treatment. Unfortunately, there continues to be insufficient awareness that the presence of a focal disturbance field can limit or cancel the effectiveness of every holistic treatment. It should be a precondition to examine the patient and to undertake sanitizations before the administration of isopathic/homeopathic preparations. Not only should the usual foci in teeth, tonsils, paranasal sinuses, intestine, etc. be considered, but also the amalgam fillings play an important part in the sense of focal toxicoses through years of releasing mercury. The replacement of these fillings by neutral materials is desirable. An article by Dr. med. A. Baum on Paravertebral Whealing points out the importance of a possible Neural or Segment Therapy. This opens many possibilities, regardless of whether one wishes to apply only the blocking infiltration methods, acupuncture, or manual forms of therapy. In diseases from the Endobiosis complex, and especially in cases of overweight, a diet rich in vitamins and vital substances, low in calories, giving concentrated nutrition, is of fundamental importance. It is a precondition, not only for the healing process, but also for the effectiveness of every isopathic and immunobiological treatment of endobiontic conditions. Nutritional intake requires special attention in cases of Endobiosis, including cancer. It should be vegetarian, rich in raw foods and devoid of superfine flour and sugar, as well as all addictive substances. With a vegetarian diet, attention must be given to include sufficient lactic acid food for the body.

The Immunobiological Preparations from the Bacterial Phase


Beside the previously described isopathic preparations of the fungal phase, the immunobiological preparations from the bacterial phase fill an important place in biological therapy: ARTHROKEHLAN A, Formol toxoid of the Propionibacterium acnes DSM 4217 ARTHROKEHLAN U, Formol toxoid of the Corynebacterium sp. DSM 4223 BOVISAN, Mycobacterium bovis LATENSIN, Bacillus cereus M.U. 345 a LEPTUCIN, Propionibacterium avidum RECARCIN, Bacillus firmus SA. C. 501 SANUKEHL Series, Hapten preparations from typical nosode germs UTILIN, Bacillus subtilis M. U. 345 UTILIN S, Mycobacterium phlei F. U. 36 The immunobiological preparations contain diverse fractions of various bacterial species, such as intact cells, cellular extracts, cell wall fragments of polysac-

15

charides. Only especially suitable strains that were cultivated under specific conditions (note strain numbers) are being applied; their effectiveness has been proven by decades of application. They are capable of stepping into the course of a physical immune reaction and to raise the immune systems capacity for response through their nonspecific stimulation. This takes place through their influencing diverse sub-populations of lymphoid and phagocytizing cells which take part in the immune functions. For instance, they indirectly take part in the structuring of humoral antibodies.

Origin and Development of the Immunobiological Preparations 1. Mycobacteria


Mycobacteria and their fragments effect a strong stimulation of the T-cell system, inducing cellular defense reactions. This is primarily utilized therapeutically in tumor diseases, among others (J. Hartmann, Therapeutikon 9, 1990). Therapy with the preparation UTILIN S goes back historically to the application of a pathogen of the sea-turtle tuberculosis for the treatment of pulmonary tuberculosis by Professor Friedmann in the 1920s. Therefore, an outstanding immunotherapy became possible, which worked similarly to the officially sanctioned BCG inoculation, but without the occasional serious side effects. This preparation was further developed into an identically effective preparation of Mycobacterium phlei from the special strain F.U. 36. In recent years, the immunostimulating properties of the cell-wall parts of the Mycobacterium have been intensively researched, whereby the equivalence of diverse mycobacterial species has been discovered. A focal point for therapy with BCG (Mycobacterium bovis) in modern tumor treatment is presented in its instillation for cancer of the bladder. Here, also, the effectiveness of the Mycobacterium phlei F.U. 36 has proven itself as comparable.

2. Bacillus Species
In folk medicine, tea decoctions using hay, excrement from cows, or peat moss have long been used, without any knowledge of their containing Bacillus subtilis as active agent. Farmers in many countries utilized hay infusions for curing intestinal diseases in cattle. As early as 1887, Metchnikoff described the growth-inhibiting effect of aerobic soil bacteria, particularly of Bacillus subtilis, in contrast to pathogens such as Streptococci, Staphylococci, Salmonella and Mycobacterium tuberculosis. Works by Ramon and Richou, as well as Jansen and Hirschmann showed in 1943/44 the antitoxic and antibiotic properties of that pathogen, which was generally referred to as Hay bacillus. However, the first reports about the oral, subcutaneous and intravenous application of Bacillus subtilis strains were published in the years 1938/39 with outstanding therapeutic results. Particularly, its effectiveness with certain pseudotubercular forms was discovered at that time. The general stimulation effect on

16

the nonspecific defensive capacity of the human organism already showed up in these beginnings of Subtilis Therapy. The name UTILIN has been used under trade mark protection for this new, special remedy since 1939. In later years, additional Bacillus strains that are closely related to Bacillus subtilis found their entry into the therapy under the terms of LATENSIN and RECARCIN. Preparations with Bacillus species have manifold immunostimulating effects. Clinical studies yielded good success in recurring diseases of the urinary passages and the breathing organs in patients with defective immune situations in food allergies, as well as other chronic diseases that were brought about by a reduced immune status (J. Hartmann, Therapeutikon 4, 1990).

3. Corynebacteria and Propionibacteria


The immunobiological preparations ARTHROKEHLAN A and ARTHROKEHLAN U were developed from the Siphonospora polymorpha bacterial cultures of Dr. von Brehmer that were made into the preparations Toxinal and Arthrisinal. Von Brehmer (1883-1958), a contemporary of Enderlein, originally devoted himself to virus research involving diseases of plants and animals. During the examination of an accidentally received human blood sample, he discovered also microorganisms that were partly moving and partly of immobile nature. He gave them the name of Siphonospora polymorpha. He was able to prove that even the smallest fluctuations of the blood pH value within the alkaline area effected the cyclogenetic upward development of the Siphonospora toward their pathological stages. However, in acidic milieu, these higher stages fall apart again into their apathogenic, tiniest developmental stages. These works brought additional proof for Enderleins publications on pleomorphism and the cyclogeny of the Endobionts released at the identical time. Beginning 1935, von Brehmer researched an avirulent Siphonospora vaccine for therapeutic purposes. The first material was obtained from a gangrenous tooth pulp and root granuloma. From these sources, von Brehmer developed the preparation Toxinal, which was applied for rheumatic arthritic diseases, neuralgia and Herpes zoster, and Arthrisinal, a formol toxoid from highly active rod cultures, with its chief area of indication, the cancer diseases. The original cultures of Dr. von Brehmers Research Institute were later purified and identified, the Propionibacteria and Corynebacteria species were then isolated from them. These improved cultures are now forming the basis of the preparations ARTHROKEHLAN A and ARTHROKEHLAN U. An additional therapeutic development with Corynebacteria followed in the application of Corynebacterium parvum for infection prophylaxis. This strain was later reclassified as Propionibacterium acnes. The activation of the monocytemacrophage system is a general characteristic of the species Propionibacterium. Its antibacterial, antiviral, antiparasitic and antitumoral action are the result.

17

The latter, in particular, have been intensively examined in the strain Propionibacterium avidum. Its stimulatory effects on the hematopoietic system qualify it in the immune therapy especially in the treatment of myelosuppressive side effects of a cytostatic or radiation therapy.

4. Sanukehl Preparations - Polysaccarides for Haptenic Therapy


The product series of SANUKEHL preparations is based on a special production process, in which the polysaccharides of bacteria and fungi are extracted. These preparations are to be considered haptens, made of typical pathogenic Nosode germs, and defined as antigen absorbers (Cornelius). Their active principle is based on the binding of the pathogen antigens or pathogen toxins. The latter are commonly mobilized out of their body depots within a therapy with corresponding nosodes. In this way they effect a first reaction. However, persistent antigens can be a considerable obstruction for a nosode therapy. In such cases, the matching SANUKEHL preparation for each nosode is to be applied as middle agent, in order to restore the full nosode efficacy. SANUKEHL Acne, Hapten from Propionibacterium acnes SANUKEHL Brucel, Hapten from Brucella melitensis SANUKEHL Cand, Hapten from Candida albicans of Serotypes A and B SANUKEHL Coli, Hapten from Escherichia coli SANUKEHL Klebs, Hapten from Klebsiella pneumoniae SANUKEHL Myc, Hapten from Mycobacterium bovis SANUKEHL Prot, Hapten from Proteus vulgaris SANUKEHL Pseu, Hapten from Pseudomonas aeruginosa SANUKEHL Salm, Hapten from Salmonella enteriditis SANUKEHL Serra, Hapten from Serratia marcescens SANUKEHL Staph, Hapten from Staphylococcus aureus SANUKEHL Strep, Hapten from Streptococcus pyogenens SANUKEHL Trich, Hapten from Trichophyton verrucosum

General Comments on Immunobiological Preparations


The purpose of applying bacterial suspensions consists in the generation of an active immunity in the living organism by artificial means. This is achieved by exerting specific and nonspecific stimulation through application of substances into the organism, which cause tissue cells to become stimulated, and the body to form defensive substances. From the type and amount of these formed substances one can then estimate the degree of currently existing immunity. To be sure, it is possible for active immunity to exist under certain circumstances, without proof that humoral bodies are circulating in the blood. However, these substances can immediately reoccur when a new impulse is given to the reactive tissue through a renewed administration of preparations or through specific or nonspecific stimulants.

18

First Immune Response


Occasionally, a first immune response occurs because the immunologic preparations contain biological substances. Therefore hypersensitivity is possible, in which case the remedy should be discontinued.

Manner of Application of Immunobiological Preparations


The preparations can either be given parenterally, that is, bypassing the gastrointestinal tract, or (orally) through the intestinal tract. The parenteral intake guarantees a good and generous immunity. One can inject subcutaneously, intramuscularly and intracutaneously. Finally, also the percutaneous and nasal administration can be used by rubbing the suspension into the skin or dropping into each nostril.

Oral Administration
The oral application of the immunobiological preparations in capsulated form, especially for certain reasons of suitability, for prophylaxis of diseases of the digestive tract, is preferred. Orally taken preparations are intended for reaching immunity and reducing sensitivity toward the relevant infectious pathogen. If a quick and lasting immunization is the target, one can first bring about a basic immunity through a subcutaneous injection. Then, this effect can be maintained and increased through oral intake.

Injection
The injecting process of the injection solution must occur slowly and under sterile conditions. Only disposable syringes are to be used.

Subcutaneous Injections
Subcutaneous injection is recommended when one targets a lasting effect through slow absorption. Therefore, this type of injection is recommended especially for prophylactic purposes, when one wishes for a maximally long lasting immunity. For the injection, one must naturally avoid locations near the periosteum or nerves and, instead, inject where the correspondingly developed subcutaneous tissue and the musculature beneath it allow for better tolerance. At the beginning of the injection treatment, 0.5 to 1.0 ml 6X are, as a rule, injected into the axillary fold.

Intramuscular Injection
The intramuscular injection is preferred when the goal is to obtain a maximally fast absorption without obtaining a larger general reaction. Therefore, it is highly recommended for therapeutic purposes, especially for suspensions that would cause subcutaneous local reactions because of the stronger active substances contained in them. For the intramuscular injection those locations are to be chosen where the strength of the musculature guarantees a fast absorption. One chooses for this the upper external quadrant of the glutea, and injects deeply intramuscular with 50 or 60 mm needles.

19

Intracutaneous Injection
The intracutaneous application is less used for stimulation therapy because it is too painful. However, because the skin is generally considered to be an important carrier of immunity, an intracutaneous administration of the suspension can in many cases be of excellent usefulness, particularly when the skin itself is the seat of disease (furunculosis, acne, etc.). Naturally, one can use only smaller dosages of 0.2-0.5 ml maximally for the intracutaneous injection, due to the size of the wheal formation and the accompanying parallel painfulness. The stretching side of the left upper or lower arm is suitable for this type of application.

Percutaneous Rubbing
Percutaneous rubbing has proven itself well in every case that involves organ stress or nervous irritation and where segmental therapy is appropriate.

The Acid-Base Equilibrium


As already mentioned, fluctuations of the blood pH value in the alkaline area which is generally preceded by a massive acidification of the tissue - give support for the upward development of the symbionts toward parasitic germination, the cause or support for diseases. It is nowadays beyond argumentation that most of civilizations diseases are conditioned by our poor nutritional habits. The unhealthy lifestyle of human beings through inappropriate nutrition with excessive ingestion of proteins makes one acidified in the actual sense of the word. The accompanying manifestations todays civilization diseases are always a mesenchymal acidosis with a simultaneously excessively raised alkaline blood pH value, a pathological acidity quotient, according to Sander, along with an extremely low defensive factor. These are sure criteria for a metabolic derailment, with the danger of an acute or chronic disease. Merely by changing ones nutrition, healthy human beings can expect a balanced acid-base maintenance by choosing a vegetarian diet. As a supportive measure for the restoration of the acid-base equilibrium, ALKALA N is the perfect treatment. For excessive acidification of the gastrointestinal tract with its consequences, such as heartburn and gas. It is important to note that all pro-ducts are calibrated to be in balance with one another. CITROKEHL brings regulatory action into cell respiration and acid-base management, by acting against the alkalosis of the blood. SANUVIS is an additional preparation for regulating the pH value of the blood and tissue, with L (+) lactic acid as its active constituent. The specialty of SANUVIS lies in the various potencies which are brought together within the preparation. The lower potencies serve the raising of cellular breathing, while the higher potencies serve the elimination of excessive lactic acid concentrations, especially of the nonphysiological D-(-) lactic acid.

Organ Preparations
20

THYMOKEHL activates the metabolism, stimulates the prestages of the T-lymphocytes to maturation and strengthens the immune system. CHRYSOCOR, a human placenta hydrolysate, contains biogenic stimulators that enter actively into the metabolism by raising the cellular respiration. REBAS, an organ extract of Peyers Patches (taken from pigs under controlled conditions and veterinary supervision) that stimulates the B- and T-lymphocytes, thus strengthening the humoral defenses, and supporting the body in the maintenance or establishment of an intact immune system.

Plant Extracts
Plant extracts are an ideal and necessary support therapy, especially since this entire homeopathic/isopathic product line (fungal, mineral & trace elements, bacterial, herbal, organ, etc.) is calibrated to be in perfect balance with one another to achieve best results. CERIVIKEHL promotes blood flow through the mucous membranes; it has, additionally, a regulatory influence on pathogens in the gastrointestinal area. GINKGOBAKEHL is based on the active constituent complex of the leaves of the Ginkgo tree, this is well known from Asian folk medicine. In RELIVORA Complex, the active substance concentrations of Drosera, Echinacea angustifolia and Juglans are ideally combined for best efficacy. Diseases of the respiratory tract, frequent general infections and diseases of the skin are a broad field for application for the RELIVORA Complex. EPISCORIT is a herbal hemeopathic immuno-stimulant, made from Echinacea purpurea expressed juice. LUFFASAN, OKOUBASAN, and USNEABASAN are also herbal homeopathic remedies. LUFFASAN, from the fruits of Luffa operculata, a sort of pumpkin, is used in homeopathy mainly for allergic rhinitis and conjunctivitis. The remedy also regulates the function of the whole intestinal system, and it raises the energy (Chi) of the kidneys. USNEABASAN, made from the lichen Usnea barbata, is predominantly used for illnesses in the head area (headaches, sunstroke) and together with LUFFASAN for the elimination of heavy metals, while OKOUBASAN, from the tree bark of Okoubaka aubrevillei, finds its application in detoxifying the gastrointestinal tract, in cases of food intolerance or, prophylactically, for changes in climate and nutrition. Besides, there are many areas of application for patients who are stressed through pesticides, insecticides, environmental disorders. These are excellent preparations for detoxification of the entire system - especially effective in the early stages of colds and flu. With these three herbal homeopathic remedies the following SANUM Elimination Cure (next page), an efficient elimination therapy for heavy metals, toxins and metabolic waste products can be performed. STROPHANTHUS 4X Sanum with its active ingredient Strophanthin, as a gen-

21

eral cardiac stimulant, has a rapid effect with a short retention time at the heart and is indicated by cardiac insufficiency and myocarditis. Hexacyl is indicated for the elemination of all toxic or infectious damage with increased degradation of protein such as food intolerance, infections and intoxications.

Mineral and Trace Element Preparations


An important factor for the maintenance of our health lies in providing the body with necessary mineral and trace elements. Regulatory processes in the organism, which are the precondition for a regulated metabolic process, cannot take their course without a stable electrolyte equilibrium of ions, such as Sodium, Potassium, Calcium and Magnesium. The trace elements, which according to their name are needed by the body in only very small amounts, enter catalytically into the metabolic processes. Without the presence of these Bio-catalysts - including Iron, Zinc, Manganese, Copper, Cobalt, Iodine and Fluorine - many processes that are essential for life cannot take their course, such as the action of the heart. These mineral and trace element preparations are offered for a broad application spectrum: ALKALA N (Na, K), MAPURIT (Mg), SELENOKEHL (Se), ZINKOKEHL (Zn), and CUPRUKEHL (Cu), and, of course, they are calibrated to a perfectly balanced total therapy with all the aforementioned products.

22

Scheme for a Basic Therapy of Chronic Diseases


1) Milieu correction by changing to a vegan diet (in particular omitting products containing cows milk, hens eggs and pork); 2) Deacidification with 1/2 measuring spoon of ALKALA N mornings and evenings dissolved in warm water orally, SANUVIS, 2 tablets suck in the morning or drink 1 tablespoonful of drops in water spread over the day and CITROKEHL 1 tablet in the evening (or 5-10 drops in water). At the same time: 3) Intestinal cleansing: FORTAKEHL 5X, 2 drops to rub in around the navel, increasing the dose to 8-10 drops rubbed in and/or orally in the morning as well as PEFRAKEHL 5X / EXMYKEHL 5X, 2-3 drops to rub in, in the evening, increasing the dosage up to 10 drops, rubbed in and/or taken orally; duration 10 to 21 days, depending on the patients discomfort; 4) Basic regulation following intestinal cleansing or at the same time with milieu corrections, depending on the clinical picture: MUCOKEHL 5X, 5 drops mornings and NIGERSAN 5X, 5 drops evenings or a combination of both, SANKOMBI 5X, mornings and evenings 5 drops each, increasing the dose up to 10 drops orally. If the basic regulation follows intestinal cleansing, it is recommended to administer SANKOMBI 5X (MUCOKEHL 5X and NIGERSAN 5X) from Monday to Friday and weekends PEFRAKEHL 5X / EXMYKEHL 5X in the prescribed dose. This rotation is followed for some weeks according to the 5-2-5-2 days pattern; 5) Immune modulation: From the 2nd week of treatment apply LATENSIN 6X, RECARCIN 6X, UTILIN 6X, and UTILIN S 6X alternating 1 capsule per week. 6) Substitution: SELENOKEHL 4X, 10 drops in the morning; MAPURIT, 1-2 capsules at noon; ZINKOKEHL 3X, 10 drops in the evening. 7) Continuation therapy: with SANUKEHL preparations (haptens), FORMASAN, CERIVIKEHL, LARIFIKEHL The above-mentioned isopathic prescriptions of FORTAKEHL, PEFRAKEHL, MUCOKEHL and NIGERSAN in 5X can be replaced by oral application with tablets whereby 1 tablet corresponds to 5 drops.

SANUM Elimination Cure


An efficient elimination therapy for heavy metals, toxins and metabolic waste products. - From Monday-Friday: Mornings 5-10 drops OKOUBASAN and USNEABASAN alternating daily (start carefully with 2-3 drops each) - Saturday and Sunday: daily 1-2 tablets LUFFASAN (start carefully with 1/2 tbl.) - Additional daily: noon 1 capsule MAPURIT, evening 10-12 drops ZINKOKEHL.

23

Albicansan 5X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Candida albicans extract 5X 1 ml liquid dilution contains: Medically active substance: 1 ml Candida albicans 5X dil. Other constituents: purified water. Strengthening of the cellular immune defense through the stimulation of the T-lymphocyte population. The isopathic effect is due to the combination of the saprophytic yeast phase with the parasitary fungal phase of Candida albicans. Mycoses and secondary mycotic, infectious skin disorders, diseases of the mouth, like stomatitis, gingivitis, perlche, aphthae, mycosis of the urogenital tract, such as vaginitis, urethritis, possibly for adnexitis. Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops before a meal. For rubbing in: 1 x daily 5-10 drops at the location of the disease or into the bend of the elbow. In case of simultaneous treatment with injections, rub in 2 x weekly 5-10 drops on injection-free days. In cases of known hypersensitivity to Candida albicans, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Albicansan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment: Advice:

Candida albicans as an active ingredient is also contained in Exmykehl. After opening, contents must be used within 2 months.
The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X, 30 g tube of ointment 3X.

How supplied:

24

Albicansan 5X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Candida albicans extract 5X 1 ampule of 1 ml contains: Medically active substance: 1 ml Candida albicans 5X aqueous dilut. Other constituents: isotonic sodium chloride solution. Strengthening of the cellular immune defense through the stimulation of the T-lymphocyte population. The isopathic effect is due to the combination of the saprophytic yeast phase with the parasitary fungal phase of Candida albicans. Mycoses and secondary mycotic, infectious skin disorders, diseases of the mouth, like stomatitis, gingivitis, perlche, aphthae, mycosis of the urogenital tract, such as vaginitis, urethritis, possibly for adnexitis. Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intramuscularly or intravenously, 2 x weekly. In cases of known hypersensitivity to Candida albicans, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Albicansan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment: Advice: How supplied:

Candida albicans as an active ingredient is also contained in Exmykehl.


The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X, 30 g tube of ointment 3X.

25

Albicansan 4X
Capsules
For oral intake

Active ingredient: Composition:

Candida albicans extract 4X 1 capsule contains: Medically active substance: 330 mg Candida albicans 4X trit. Other constituents: lactose, hypromellosis (capsule shell) Strengthening of the cellular immune defense through the stimulation of the T-lymphocyte population. The isopathic effect is due to the combination of the saprophytic yeast phase with the parasitary fungal phase of Candida albicans. Mycoses and secondary mycotic, infectious skin disorders, diseases of the mouth, like stomatitis, gingivitis, perlche, aphthae, mycosis of the urogenital tract, such as vaginitis, urethritis, possibly for adnexitis. Unless otherwise prescribed: 1-3 capsules daily, either before breakfast or at bedtime, taken with some liquid. In cases of known hypersensitivity to Candida albicans, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Albicansan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment: Advice: How supplied:

Candida albicans as an active ingredient is also contained in Exmykehl.


The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X, 30 g tube of ointment 3X.

26

Albicansan 3X
Suppositories

Active ingredient: Composition:

Candida albicans extract 3X 1 suppository contains: Medically active substance: 0.2 g Candida albicans 3X trit. Other constituents: hard fat, lactose. Strengthening of the cellular immune defense through the stimulation of the T-lymphocyte population. The isopathic effect is due to the combination of the saprophytic yeast phase with the parasitary fungal phase of Candida albicans. Mycoses and secondary mycotic, infectious skin disorders, diseases of the mouth, like stomatitis, gingivitis, perlche, aphthae, mycosis of the urogenital tract, such as vaginitis, urethritis, possibly for adnexitis. Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally at bedtime. In cases of known hypersensitivity to Candida albicans, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Albicansan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment: Advice: How supplied:

Candida albicans as an active ingredient is also contained in Exmykehl.


The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X, 30 g tube of ointment 3X.

27

Albicansan 3X
Ointment

Active ingredient: Composition:

Candida albicans extract 3X 1 g ointment contains: Medically active substance: 0.1 g Candida albicans 3X dil. Other constituents: 0.38 g Lanolin alcohol ointment, 0.1 g Coconut oil fract., 0.03 g Glyceryl monostearate 40-50%, 0.23 g Propylene glycol, 0.02 g Magnesium sulphate x 7 H2O, 0.01 g Lactic acid, 0.13 g water for injection. Strengthening of the cellular immune defense through the stimulation of the T-lymphocyte population. The isopathic effect is due to the combination of the saprophytic yeast phase with the parasitary fungal phase of Candida albicans. Mycoses and secondary mycotic, infectious skin disorders, balanitis, pruritus genitalis

Characteristics:

According to experience, to be administered in cases of: Application: Contraindications:

Unless otherwise prescribed: Apply on the affected area 1 to 3x daily. In cases of known hypersensitivity to Candida albicans, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Albicansan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment: Advice: How supplied:

Candida albicans as an active ingredient is also contained in Exmykehl.


The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X, 30 g tube of ointment 3X.

28

Alkala N
Powder

Active ingredients: Composition:

sodium bicarbonate, sodium citrate, potassium bicarbonate 150 g powder contain: 2.67 g sodium citrate x H2O, 13.40 g potassium bicarbonate, 133.93 g sodium bicarbonate. Alkala N is a base mixture, excellently suited for correction of the acidbase balance in the organism. Ideally this relation is balanced in the human being. Dislocations of the acid-base balance towards the acid range are nowadays more frequent through outliving and environmental conditions. The first typical symptoms for hyperacidity in the stomach and intestinal area are heartburn, acid regurgitation, flatulence, etc. Subsequently hyperacidity is a typical accompanying symptom of the chronical metabolic disorders which can result in degeneration of the cells. Alkalization, acidosis of the stomach and the duodenum, heartburn, gastritis and ulcus ventriculi, liver and gallbladder troubles, repletion and flatulence, rheumatic diseases, chronic skin diseases and diseases of the respiratory and urogenital tract Take 1 level spoonful of Alkala N powder from the measuring spoon provided dissolved in 1/2 glass of liquid in the morning. The prescribed dosage can also be taken little and often during the course of the day. Anacidity of the stomach. None known. The absorption and excretion of weak acids and bases can be influenced through the increasing pH value in the stomach and urine. Functional interactions are possible with gluco- and mineralocorticoids, androgens and diuretics which increases the excretion of potassium. Frequently repletion and eructation. Long term use promotes the development of calcium and magnesium phosphate kidney stones. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. In case of disturbed excretion (anuria, renal insufficiency) and exsiccation (exsiccosis through water deficiency) as well as in alcalosis Alkala N should only be taken under medical supervision. Container with 150 g powder, multiple package with 60 x 150 g.

Characteristics:

Indications:

Application:

Contraindications: Adverse reactions: Interactions with other remedies:

Side effects:

Precautions:

Advice:

How supplied:

29

Arthrokehlan A 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Propionibacterium acnes extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Propionibacterium acnes 6X dil. Other constituents: purified water. Arthrokehlan A is gained through the cultivation of Siphonospora polymorpha which have been isolated from the bacterial flora of human dental granuloma. In accordance with Dr. v. Brehmers method, a formol toxoid (a detoxified culture filtrate) is produced from these cultures. It effects a sustained rise in the defensive capacity. Arthritic, arthrotic, as well as degenerative diseases of the spinal column and the entire apparatus of locomotion, myalgia.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops before a meal. For rubbing in: 1 x daily 5-10 drops at the location of the disease or into the bend of the elbow. In cases of known hypersensitivity to Propionibacterium acnes, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Arthrokehlan A, hypersensitivity theoretically may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. Arthrokehlan A was previously marketed under the names SpezialAnatoxin A and Arthrisinal. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 6X.

Duration of treatment: Advice:

How supplied:

30

Arthrokehlan A 6X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Propionibacterium acnes extract 6X 1 ampule of 1 ml contains: Medically active substance: 1 ml Propionibacterium acnes 6X aqueous dilut. Other constituents: isotonic sodium chloride solution. Arthrokehlan A is gained through the cultivation of Siphonospora polymorpha which have been isolated from the bacterial flora of human dental granuloma. In accordance with Dr. v. Brehmers method, a formol toxoid (a detoxified culture filtrate) is produced from these cultures. It effects a sustained rise in the defensive capacity. Arthritic, arthrotic, as well as degenerative diseases of the spinal column and the entire apparatus of locomotion, myalgia.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 0.2-1.0 ml to be injected deep intramuscularly - regular intragluteally - at the lying patient, 2-3 x weekly. In case of strong reactions, injections have to be discontinued; the treatment can be continued with the dosage form drops. As a general advice the dosage has to be chosen adequately, so that strong general reactions do not occur and that the local reactions are confined to the site of injections. Fever, conditions of weakness. In cases of known hypersensitivity to Propionibacterium acnes, as a precaution, this preparation should not be administered. None known. Generally well tolerated. Occasionally local reactions like rubefaction, swelling or painfulness may be observed, normally vanishing without treatment. These effects are not to be seen as adverse reactions, but rather as an expression of effectiveness. In the first 2 or 3 days after the injection sometimes conditions of weakness, fortified expectoration, slight painfulness of the region or subfebrile temperatures may show. Strong general reactions are always a sign of overdosage or of incorrect injection technique. None known. An interval of four weeks should be kept to the administration of vaccinations. In cases of simultaneous treatment with immunosuppressive remedies, the effectiveness of Arthrokehlan A may be influenced. None known.

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects:

31

Precautions:

As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. Arthrokehlan A was previously marketed under the names SpezialAnatoxin A and Arthrisinal. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 6X.

Duration of treatment: Advice:

How supplied:

32

Arthrokehlan U 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Corynebacterium sp. extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Corynebacterium sp. 6X dil. Other constituents: purified water. Arthrokehlan U is gained through the cultivation of Siphonospora polymorpha, which have been isolated from dental granuloma, teeth with diseased pulp and tonsils. In accordance with Dr. v. Brehmers method, a formol toxoid (a detoxified culture filtrate) is produced from these cultures. After intramuscular injection, it effects a sustained rise in the defensive capacity. Stimulation of endogenic defense capacities, adjuvant in anti-carcinomatous therapy.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops before a meal. For rubbing in: 1 x daily 5-10 drops at the location of the disease or into the bend of the elbow. In cases of known hypersensitivity to Corynebacterium sp., as a precaution, this preparation should not be administered. None known. Because of specific organic components of Arthrokehlan U, hypersensitivity theoretically may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. Arthrokehlan U was previously marketed under the names SpezialAnatoxin U, Arthrisinal U and Toxinal. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 6X.

Duration of treatment: Advice:

How supplied:

33

Arthrokehlan U 6X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Corynebacterium sp. extract 6X 1 ampule of 1 ml contains: Medically active substance: 1 ml Corynebacterium sp. 6X aqueous dilut. Other constituents: isotonic sodium chloride solution. Arthrokehlan U is gained through the cultivation of Siphonospora polymorpha, which have been isolated from dental granuloma, teeth with diseased pulp and tonsils. In accordance with Dr. v. Brehmers method, a formol toxoid (a detoxified culture filtrate) is produced from these cultures. After intramuscular injection, it effects a sustained rise in the defensive capacity. Stimulation of endogenic defense capacities, adjuvant in anti-carcinomatous therapy.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 0.2-1.0 ml to be injected deep intramuscularly - regular intragluteally - at the lying patient, 2-3 x weekly. Normally the treatment is started with the administration of drops. In case of absent or weak reactions the dosage may be gradually raised. In case of strong reactions, injections have to be discontinued; the treatment can be continued with the dosage form drops. As a general advice the dosage has to be chosen adequately, so that strong general reactions do not occur and that the local reactions are confined to the site of injections. Fever, conditions of weakness. In cases of known hypersensitivity to Corynebacterium sp., as a precaution, this preparation should not be administered. None known. Generally well tolerated. Occasionally local reactions like rubefaction, swelling or painfulness may be observed, normally vanishing without treatment. These effects are not to be seen as adverse reactions, but rather as an expression of effectiveness. In the first 2 or 3 days after the injection sometimes conditions of weakness, fortified expectoration, slight painfulness of the region or subfebrile temperatures may show. Strong general reactions are always a sign of overdosage or of incorrect injection technique. None known. An interval of four weeks should be kept to the administration of vaccinations. In cases of simultaneous treatment with immunosuppressive remedies, the effectiveness of Arthrokehlan U may be influenced.

Contraindications:

Adverse reactions:

Interactions with other remedies:

34

Side effects: Precautions:

None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. Arthrokehlan U was previously marketed under the names SpezialAnatoxin U, Arthrisinal U and Toxinal. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 6X.

Duration of treatment: Advice:

How supplied:

35

Bovisan 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Mycobacterium bovis (BCG) extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Mycobacterium bovis (BCG) 6X dil. Other constituents: purified water. A. Calmette and G. Guerin have described the production of a primary solution of Mycobacterium tuberculosis var. bovis between 1911 and 1914. After a long and very particular preparation, this solution exhibits an avirulent condition, without losing its antigenic properties. This suspension of weakened bacilli is applied for inoculation, and it gives rise to a positive cutaneous reaction. The homeopathic production is based on an extract of this bacterial strain which, on the one hand, does not have any infectiousness - as common vaccines do - and, on the other hand, has extraordinary immunomodulating characteristics. Inflammation after BCG prophylactic vaccination, hypertrophy of the tonsils, erythema nosodum, tuberculous rheumatism after Poncet-Leriche, articular rheumatism, asthenia with chronic hypotonia, for immune modulation. Unless otherwise prescribed: For oral intake: 1-3 x daily 2-5 drops before a meal. For rubbing in: 2-3 x weekly 5-10 drops at the location of the disease or into the bend of the elbow. In cases of known hypersensitivity to Mycobacterium bovis, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Bovisan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 6X, 5 capsules 5X, 10 suppositories 5X.

Duration of treatment: How supplied:

36

Bovisan 6X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Mycobacterium bovis (BCG) extract 6X 1 ampule of 1 ml contains: Medically active substance: 1 ml Mycobacterium bovis (BCG) 6X aqueous dilut. Other constituents: isotonic sodium chloride solution. A. Calmette and G. Guerin have described the production of a primary solution of Mycobacterium tuberculosis var. bovis between 1911 and 1914. After a long and very particular preparation, this solution exhibits an avirulent condition, without losing its antigenic properties. This suspension of weakened bacilli is applied for inoculation, and it gives rise to a positive cutaneous reaction. The homeopathic production is based on an extract of this bacterial strain which, on the one hand, does not have any infectiousness - as common vaccines do - and, on the other hand, has extraordinary immunomodulating characteristics. Inflammation after BCG prophylactic vaccination, hypertrophy of the tonsils, erythema nodosum, tuberculous rheumatism after Poncet-Leriche, articular rheumatism, asthenia with chronic hypotonia, for immune modulation. Unless otherwise prescribed: 1 ampule of 1 ml to be injected deep intramuscularly - regular intragluteally - while the patient is lying down, every two weeks. Normally the treatment is started with the administration of drops 6X or capsules 5X. In case of absent or weak reactions the dosage may be gradually raised by shorter intervals - 2 ampules weekly at the most. In case of strong reactions, injections have to be discontinued; the treatment can be continued with the dosage forms drops and capsules. As a general advice the dosage has to be chosen adequately, so that strong general reactions do not occur and that local reactions are confined to the site of injections. Fever, conditions of weakness. In cases of known hypersensitivity to Mycobacterium bovis, as a precaution, this preparation should not be administered.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

37

Adverse reactions:

None known. Generally well tolerated. Occasionally local reactions like rubefaction, swelling or painfulness may be observed, normally vanishing without treatment. These effects are not to be seen as adverse reactions, but rather as an expression of effectiveness. In the first 2 or 3 days after the injection, sometimes conditions of weakness, fortified expectoration, slight painfulness of the region or subfebrile temperatures may occur. Strong general reactions are always a sign of overdosage or of incorrect injection technique. In this case the treatment can be continued orally with Bovisan drops or capsules. None known. An interval of four weeks should be kept to the administration of vaccinations. In cases of simultaneous treatment with immunosuppressive remedies, the effectiveness of Bovisan may be influenced. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. Shake well before use. Bovisan is employed as an irritative agent for all subacute to chronic relapsing infections in isopathic therapy, especially in the region of the head. Before the administration of Bovisan, an increased toxin elimination is important. Under the noticeable stimulus threshold, a good effect of Bovisan is also achieved. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 6X, 5 capsules 5X, 10 suppositories 5X.

Interactions with other remedies:

Side effects: Precautions:

Duration of treatment: Advice:

How supplied:

38

Bovisan 5X
Capsules
For oral intake

Active ingredient: Composition:

Mycobacterium bovis (BCG) extract 5X 1 capsule contains: Medically active substance: 330 mg Mycobacterium bovis 5X trit. Other constituents: lactose, hypromellosis (capsule shell) A. Calmette and G. Guerin have described the production of a primary solution of Mycobacterium tuberculosis var. bovis between 1911 and 1914. After a long and very particular preparation, this solution exhibits an avirulent condition, without losing its antigenic properties. This suspension of weakened bacilli is applied for inoculation, and it brings forth a positive cutaneous reaction. The homeopathic production is based on a cell-wall preparation of this bacterial strain which, on the one hand, does not have any infectiousness - as common vaccines do - and, on the other hand, has extraordinary immunomodulating characteristics. Inflammation after BCG prophylactic vaccination, hypertrophy of the tonsils, erythema nosodum, tuberculous rheumatism after Poncet-Leriche, articular rheumatism, asthenia with chronic hypotonia, for immune modulation. Unless otherwise prescribed: 1 capsule every two weeks in the morning before breakfast or at bedtime, taken with some liquid. If the reaction is weak or missing the dosage can be raised to 2 per week maximum. In cases of known hypersensitivity to Mycobacterium bovis, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Bovisan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 6X, 5 capsules 5X, 10 suppositories 5X.

Duration of treatment: How supplied:

39

Bovisan 5X
Suppositories

Active ingredient: Composition:

Mycobacterium bovis (BCG) extract 5X 1 suppository contains: Medically active substance: 0.2 g Mycobacterium bovis (BCG) 5X trit. Other constituents: hard fat, lactose. A. Calmette and G. Guerin have described the production of a primary solution of Mycobacterium tuberculosis var. bovis between 1911 and 1914. After a long and very particular preparation, this solution exhibits an avirulent condition, without losing its antigenic properties. This suspension of weakened bacilli is applied for inoculation, and it gives rise to a positive cutaneous reaction. The homeopathic production is based on a cell-wall preparation of this bacterial strain which, on the one hand, does not have any infectiousness - as common vaccines do - and, on the other hand, has extraordinary immunomodulating characteristics. Inflammation after BCG prophylactic vaccination, hypertrophy of the tonsils, erythema nosodum, tuberculous rheumatism after Poncet-Leriche, articular rheumatism, asthenia with chronic hypotonia, for immune modulation. Unless otherwise prescribed: 1-3 x weekly 1 suppository, inserted into the rectum at bedtime. In cases of known hypersensitivity to Mycobacterium bovis, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Bovisan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 6X, 5 capsules 5X, 10 suppositories 5X.

Duration of treatment: How supplied:

40

Calvakehl 3X
Drops
Liquid dilution for oral intake

Active ingredient: Composition:

Calvatia gigantea extract 3X 1 ml liquid dilution contains: Medically active substance: 1 ml Calvatia gigantea 3X dil. Other constituents: purified water, ethanol. Calvakehl is a plant remedy produced from the Giant bovista fungus. In 16th century, the application was already well known in folk medicine for its hemostyptic and wound healing properties. Bleeding dispositions, as in nose or uterus; weakness of the heart and circulatory system with blood congestion; lack of oxygen in blood; skin rashes; indigestion and diarrhea. Unless otherwise prescribed: 1-3 x daily 5-10 drops. In cases of known hypersensitivity to Calvatia gigantea, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Calvakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application: Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The preparation contains 70 % (v/v) alcohol (ethanol). The following dosage forms are available: 10 ml and 30 ml dropper bottle 3X, 80 tablets 4X.

Duration of treatment: Advice: How supplied:

41

Calvakehl 4X
Tablets

Active ingredient: Composition:

Calvatia gigantea extract 4X 1 tablet contains: Medically active substance: 250 mg Calvatia gigantea 4X trit. Other constituents: lactose, potato starch, magnesium stearate. Calvakehl is a plant remedy produced from the Giant bovista fungus. In the 16th century, its application was already well known in folk medicine for its hemostyptic and wound healing properties. Bleeding dispositions, as in nose or uterus; weakness of the heart and circulatory system with blood congestion; lack of oxygen in blood; skin rashes; indigestion and diarrhea. Unless otherwise prescribed: 1-3 x daily 1-2 tablets at bedtime. In cases of known hypersensitivity to Calvatia gigantea, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Calvakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application: Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml and 30 ml dropper bottle 3X, 80 tablets 4X.

Duration of treatment: How supplied:

42

Cerivikehl 1X
Drops
Liquid dilution for oral intake

Active ingredient: Composition:

Cetraria islandica extract mother tincture 1 ml liquid dilution contains: Medically active substance: 1 ml Cetraria islandica 1X dil. Other constituents: purified water, ethanol. Cerivikehl, a plant remedy made of the lichen called Icelandic Moss is generally used for the promotion of the circulation of the mucous membranes. A certain constituent of the lichen acids manifests a mild antibiotic action toward pathogens in oral-, pharyngeal- and intestinal infections; it is not known to cause resistant allergic reactions or resistance of bacteria to antibiotics. Diseases of the respiratory system, sinusitis, laryngitis, bronchitis, dry cough, lack of appetite.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: In case of acute conditions: 5 drops every half to one hour. In case of chronic forms: 1-3 x daily 5-10 drops. None known. None known. Because of specific organic components of Cerivikehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications: Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The preparation contains 70 % (v/v) alcohol (ethanol). The following dosage forms are available: 30 ml dropper bottle 1X, 2 ml ampule 10 and 50 3X.

Duration of treatment: Advice: How supplied:

43

Cerivikehl 3X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Cetraria islandica extract 3X 1 ampule of 2 ml contains: Medically active substance: 2 ml Cetraria islandica 3X aqueous dilut. Other constituents: isotonic sodium chloride solution. Cerivikehl, a plant remedy made of the lichen called Icelandic Moss is generally used for the promotion of the circulation of the mucous membranes. A certain constituent of the lichen acids manifests a mild antibiotic action toward pathogens in oral-, pharyngeal- and intestinal infections; it is not known to cause resistant allergic reactions or resistance of bacteria to antibiotics. Diseases of the respiratory system, sinusitis, laryngitis, bronchitis, dry cough, lack of appetite.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 2 ml to be injected either intramuscularly, subcutaneously, intracutaneously or intravenously, 1 x daily. None known. None known. Because of specific organic components of Cerivikehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications: Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 30 ml dropper bottle 1X, 2 ml ampule 10 and 50 3X.

Duration of treatment: How supplied:

44

Chrysocor 3X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Placenta hydrolysate extract (human) 3X 1 ampule of 2 ml contains: Medically active substance: 2 ml placenta hydrolysate (human) 3X aqueous dilut. Other constituents: isotonic sodium chloride solution. Chrysocor is a human placenta hydrolysate implemented for the stimulation of the metabolism. According to Filatow, a placenta extract contains biogenic stimulators, which has an activating effect on metabolic processes, particularly the general oxidation process in the organism (cellular respiration). Constituents of placenta extracts are amino acids and in particular peptides with hormone-like characters. The content of potentially allergenic substances in Chrysocor has been strongly reduced by a special production process (low protein content). Functional disorders of the male gonads, conditioned by disease or old age, climacterium virile, sexual adynamia, sexual asthenia, hypogenitalism, adjuvant for cellular regeneration therapy. Unless otherwise prescribed: It is started with 1 ml each second day and increased slowly to 2 ml. The dose is to be injected deep intramuscularly (intragluteally) in the lying patient. In cases of known hypersensitivity to foreign protein, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Chrysocor, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 2 ml ampule 10 and 50 3X, 5X.

Duration of treatment: How supplied:

45

Chrysocor 5X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Placenta hydrolysate (human) extract 5X 1 ampule of 2 ml contains: Medically active substance: 2 ml placenta hydrolysate (human) 5X aqueous dilut. Other constituents: isotonic sodium chloride solution. Chrysocor is a human placenta hydrolysate implemented for the stimulation of the metabolism. According to Filatow, a placenta extract contains biogenic stimulators, which has an activating effect on metabolic processes, particularly the general oxidation process in the organism (cellular respiration). Constituents of placenta extracts are amino acids and in particular peptides with hormone-like characters. The content of potentially allergenic substances in Chrysocor has been strongly reduced by a special production process (low protein content). Functional disorders of the male gonads, conditioned by disease or old age, climacterium virile, sexual adynamia, sexual asthenia, hypogenitalism, adjuvant for cellular regeneration therapy. Unless otherwise prescribed: It is started with 1 ml each second day and increased slowly to 2 ml. The dose is to be injected deep intramuscularly (intragluteally) in the lying patient. In cases of known hypersensitivity to foreign protein, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Chrysocor, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 2 ml ampule 10 and 50 3X, 5X.

Duration of treatment: How supplied:

46

Citrokehl 10X/30X/200X
Drops
Liquid dilution for oral intake

Active ingredient: Composition:

Acidum citricum 10X/30X/200X 100 ml liquid dilution contains: Medically active substance: 33.4 ml Acidum citricum 10X dil., 33.4 ml Acidum citricum 30X dil., 33.4 ml Acidum citricum 200X dil. Other constituents: purified water, ethanol.

Characteristics:

Acidum citricum (citric acid), the active ingredient of Citrokehl, is an important link in the physiological citric acid cycle. It activates vesicular breathing and is of particular importance to cell metabolism. According to the thorough examinations of Dr. Moermann, citric acid is indispensable for the human body because it counteracts the alcalosis of blood, slows down the fermentation metabolism and the fermentation of lactic acid, decreases the viscosity of blood and reduces the water content of tissues.
According to the importance of citric acid in the citric-acid-cycle of every cell, Citrokehl can be prescribed for every disease, from the acute phase up to the wasting stage of cancer. For chronic infections, allergic diseases and rheumatic diseases, gastrointestinal dysfunction, such as cholangitis, dysbacteria, as adjuvant in periodontosis and avitaminosis, as a supportive therapy in all neoplastic phases. Unless otherwise prescribed: 3 x daily 60 drops (approx. one teaspoon) before a meal. None known. None known.

According to experience, to be administered in cases of:

Application:

Contraindications: Adverse reactions: Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

47

Advice:

Citrokehl is an accompanying therapeutic agent in isopathic therapy. It is used for all therapies with derivatives of the Aspergillus type as well as for all chronic diseases which are ascribed to an oxygen deficiency of the affected tissue. This preparation contains 12.4 % (v/v) alcohol (ethanol). The following dosage forms are available: 100 ml dropper bottle 10X/30X/ 200X potency mixture, 2 ml ampule 10 and 50 10X/30X/200X potency mixture, 80 tablets 10X/30X/200X potency mixture.

How supplied:

48

Citrokehl 10X/30X/200X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Acidum citricum 10X/30X/200X 1 ampule of 2 ml contains: Medically active substance: 671 mg Acidum citricum 10X aqueous dilut., 671 mg Acidum citricum 30X aqueous dilut., 671 mg Acidum citricum 200X aqueous dilut. Other constituents: isotonic sodium chloride solution.

Characteristics:

Acidum citricum (citric acid), the active ingredient of Citrokehl, is an important link in the physiological citric acid cycle. It activates vesicular breathing and is of particular importance to cell metabolism. According to the thorough examinations of Dr. Moermann, citric acid is indispensable for the human body because it counteracts the alkalosis of blood, slows down the fermentation metabolism and the fermentation of lactic acid, decreases the viscosity of blood and reduces the water content of tissues.
According to the importance of citric acid in the citric-acid-cycle of every cell, Citrokehl can be prescribed for every disease, from the acute phase up to the wasting stage of cancer. For chronic infections, allergic diseases and rheumatic diseases, gastrointestinal dysfunction, such as cholangitis, dysbacteria, as adjuvant in periodontosis and avitaminosis, as a supportive therapy in all neoplastic phases. Unless otherwise prescribed: 1 ampule of 2 ml to be injected intramuscularly 1-3 x weekly. None known. None known.

According to experience, to be administered in cases of:

Application:

Contraindications: Adverse reactions: Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

49

Advice:

Citrokehl is an accompanying therapeutic agent in isopathic therapy. It is used for all therapies with derivatives of the Aspergillus type as well as for all chronic diseases which are ascribed to an oxygen deficiency of the affected tissue. Citrokehl and Nigersan are therefore often administered as a mixed injection. The following dosage forms are available: 100 ml dropper bottle 10X/30X/ 200X potency mixture, 2 ml ampule 10 and 50 10X/30X/200X potency mixture, 80 tablets 10X/30X/200X potency mixture.

How supplied:

50

Citrokehl 10X/30X/200X
Tablets

Active ingredient: Composition:

Acidum citricum 10X/30X/200X 1 tablet contains: Medically active substance: 83.4 mg Acidum citricum 10X trit., 83.4 mg Acidum citricum 30X trit., 83.4 mg Acidum citricum 200X trit. Other constituents: lactose, potato starch, magnesium stearate.

Characteristics:

Acidum citricum (citric acid), the active ingredient of Citrokehl, is an important link in the physiological citric acid cycle. It activates vesicular breathing and is of particular importance to cell metabolism. According to the thorough examinations of Dr. Moermann, citric acid is indispensable for the human body because it counteracts the alkalosis of blood, slows down the fermentation metabolism and the fermentation of lactic acid, decreases the viscosity of blood and reduces the water content of tissues.
According to the importance of citric acid in the citric-acid-cycle of every cell, Citrokehl can be prescribed for every disease, from the acute phase up to the wasting stage of cancer. For chronic infections, allergic diseases and rheumatic diseases, gastrointestinal dysfunction, such as cholangitis, dysbacteria, as adjuvant in periodontosis and avitaminosis, as a supportive therapy in all neoplastic phases. Unless otherwise prescribed: 1-3 x daily 1-2 tablets. None known. None known.

According to experience, to be administered in cases of:

Application: Contraindications: Adverse reactions: Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

51

Advice:

Citrokehl is an accompanying therapeutic agent in isopathic therapy. It is used for all therapies with derivatives of the Aspergillus type as well as for all chronic diseases which are ascribed to an oxygen deficiency of the affected tissue. The following dosage forms are available: 100 ml dropper bottle 10X/30X/ 200X potency mixture, 2 ml ampule 10 and 50 10X/30X/200X potency mixture, 80 tablets 10X/30X/200X potency mixture.

How supplied:

52

Cuprukehl 3X
Drops
Liquid dilution for oral intake

Active ingredient: Composition:

Copper gluconate 3X 1 ml liquid dilution contains: Medically active substance: 0.08 ml copper gluconate 3X dil. Other constituents: purified water, ethanol. Copper is an essential trace element that is vital for the human body. It is necessary in the metabolism for the function of diverse proteins and oxidative enzymes. It is indispensable for the synthesis of hemoglobin, healthy functioning nerves and formation of bones, as well as promoting the development of connective tissue for the hearts circulatory system. According to the recommendations of the World Health Organization, WHO, the human body requires 2-3 g of copper daily. Examinations carried out in the USA have shown that only 25% of people tested actually receive the recommended amounts of trace elements in their daily food intake. The reason for this is, whilst during the preparation of food, a large proportion of trace elements including copper are destroyed when cooked for too long. Clinical situations which may lead to a copper deficiency are premature births, patients supplied entirely with parenteral nutrition and children living on substandard nutrition. The capacity of the granulocytes for phagocytosis and the formation of immunoglobulins is decreased by a deficiency in copper. Inflammatory processes in the stomach, intestines and kidneys, pre- and postoperative phases.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: In case of acute conditions: 5 drops every half to one hour. In case of chronic forms: 5-10 drops 1-3 x daily. None known. None known.

Contraindications: Adverse reactions: Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

53

Duration of treatment: Advice: How supplied:

Dependent on the advice of the physician or health care professional. The preparation contains 20 % (v/v) alcohol (ethanol). The following dosage forms are available: 30 ml dropper bottle 3X, 2 ml ampule 10 and 50 4X.

54

Cuprukehl 4X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Copper gluconate 4X 1 ampule of 2 ml contains: Medically active substance: 2 ml copper gluconate 4X aqueous dilut. Other constituents: isotonic sodium chloride solution. Copper is an essential trace element that is vital for the human body. It is necessary in the metabolism for the function of diverse proteins and oxidative enzymes. It is indispensable for the synthesis of hemoglobin, healthy functioning nerves and formation of bones, as well as promoting the development of connective tissue for the hearts circulatory system. According to the recommendations of the World Health Organization, WHO, the human body requires 2-3 g of copper daily. Examinations carried out in the USA have shown that only 25% of people tested actually receive the recommended amounts of trace elements in their daily food intake. The reason for this is, whilst during the preparation of food, a large proportion of trace elements including copper are destroyed when cooked for too long. Clinical situations which may lead to a copper deficiency are premature births, patients supplied entirely with parenteral nutrition and children living on substandard nutrition. The capacity of the granulocytes for phagocytosis and the formation of immunoglobulins is decreased by a deficiency in copper. Inflammatory processes in the stomach, intestines and kidneys, pre- and postoperative phases.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 2 ml to be injected either intramuscularly, subcutaneously, intracutaneously or intravenously, 1 x daily. None known. None known.

Contraindications: Adverse reactions: Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

55

Duration of treatment: How supplied:

Dependent on the advice of the physician or health care professional. The following dosage forms are available: 30 ml dropper bottle 3X, 2 ml ampule 10 and 50 4X.

56

Episcorit 1X
Drops
Liquid dilution for oral intake

Active ingredient: Composition:

Expressed juice from fresh, blooming Echinacea purpurea 100 ml liquid dilution contains: Medically active substance: 75.6 ml expressed juice from fresh, blooming Echinacea purpurea herbs (1.5 - 2.5 : 1). Other constituents: ethanol. The origin of Echinacea purpurea is North America, where its wound healing properties was preferred by the Indians. Echinacea preparations have an immunobiological effect on humans. Echinacea stimulates the production of the endogenic interferon and therefore considerably increases the defensive mechanism. Amongst others they increase the number of leukocytes and splenocytes. Support of treatments of recurrent infections of the respiratory and urinary tracts.

Characteristics:

According to experience, to be administered in cases of: Application: Contraindications:

Unless otherwise prescribed: Adults 3-4 x daily 55 drops (= 2.75 ml). Echinacea expressed juices should not be taken if allergies to compositae are known. The remedy should not be used if progressive systemic diseases such as tuberculosis, leukemia or diseases similar to leukemia (leucosis), rheumatic diseases of the connective tissue (collagenosis), multiple sclerosis, diseases and/or infections caused by the AIDS or HIV virus, and other auto-immune diseases are known. None known.

Adverse reactions: Interactions with other remedies: Side effects:

None known. Hypersensitivity reactions may occur in individual cases. It has been observed that remedies containing Echinacea purpurea can cause exanthema, pruritus or in rare cases facial swelling, difficult breathing, vertigo and drop in blood pressure. In this case, discontinue medication and treat symptomatically. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

Precautions:

57

Duration of treatment: Advice:

Not longer than 8 weeks. Patients suffering from alcoholism or liver diseases should be aware that Episcorit contains 22 Vol.% alcohol. The amount of alcohol per dose for adults is equivalent to approximately one teaspoon. After opening, contents must be used within four weeks. The following dosage forms are available: 30 ml and 100 ml dropper bottle 1X.

How supplied:

58

Exmykehl 5X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredients:

Candida albicans extract 5X, Candida parapsilosis extract 5X, Penicillium roquefortii extract 5X 1 ml liquid dilution contains: Medically active substances: 0.334 ml Candida albicans 5X dil., 0.334 ml Candida parapsilosis 5X dil., 0.334 ml Penicillium roquefortii 5X dil. Other constituents: purified water. Exmykehl is a combination of three specific antimycotic preparations: Penicillium roquefortii, Candida parapsilosis and Candida albicans. With Candida albicans, the dimorphism phenomenon of the saprophytic parasitary development phases is included in the action of Exmykehl. The acting specificity is characterized by the broad basis of the isopathic preparations and also by the depth of the targeted effect. Intestinal mycosis, vaginal mycosis, prostate hypertrophy.

Composition:

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops before a meal. For rubbing in: 1 x daily 5-10 drops at the location of the disease or into the bend of the elbow. In case of simultaneous treatment with injections, rub in 2 x weekly 5-10 drops on injection-free days. In cases of known hypersensitivity to Candida albicans, Candida parapsilosis or Penicillium roquefortii, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Exmykehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X.

Duration of treatment: How supplied:

59

Exmykehl 5X
Ampules
Liquid dilution for injection

Active ingredients:

Candida albicans extract 5X, Candida parapsilosis extract 5X, Penicillium roquefortii extract 5X 1 ampule of 1 ml contains: Medically active substances: 0.334 ml Candida albicans 5X aqueous dilut., 0.334 ml Candida parapsilosis 5X aqueous dilut., 0.334 ml Penicillium roquefortii 5X aqueous dilut. Other constituents: isotonic sodium chloride solution. Exmykehl is a combination of three specific antimycotic preparations: Penicillium roquefortii, Candida parapsilosis and Candida albicans. With Candida albicans, the dimorphism phenomenon of the saprophytic parasitary development phases is included in the action of Exmykehl. The acting specificity is characterized by the broad basis of the isopathic preparations and also by the depth of the targeted effect. Intestinal mycosis, vaginal mycosis, prostate hypertrophy.

Composition:

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intramuscularly or intravenously, 2 x weekly. In cases of known hypersensitivity to Candida albicans, Candida parapsilosis or Penicillium roquefortii, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Exmykehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X.

Duration of treatment: How supplied:

60

Exmykehl 3X
Suppositories

Active ingredients:

Candida albicans extract 3X, Candida parapsilosis extract 3X, Penicillium roquefortii extract 3X 1 suppository contains: Medically active substances: 0.067 g Candida albicans 3X trit., 0.067 g Candida parapsilosis 3X trit., 0.067 g Penicillium roquefortii 3X trit. Other constituents: hard fat, lactose. Exmykehl is a combination of three specific antimycotic preparations: Penicillium roquefortii, Candida parapsilosis and Candida albicans. With Candida albicans, the dimorphism phenomenon of the saprophytic parasitary development phases is included in the action of Exmykehl. The acting specificity is characterized by the broad basis of the isopathic preparations and also by the depth of the targeted effect. Intestinal mycosis, vaginal mycosis, prostate hypertrophy.

Composition:

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally at bedtime. In cases of known hypersensitivity to Candida albicans, Candida parapsilosis or Penicillium roquefortii, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Exmykehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X.

Duration of treatment: How supplied:

61

Fomepikehl 5X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredients: Composition:

Fomitopsis pinicola extract 5X 1 ml liquid dilution contains: Medically active substance: 1 ml Fomitopsis pinicola 5X dil. Other constituents: purified water. According to the latest studies, polysaccarid extracts from Fomitopsis pinicola prove to be highly effective immune modulators. Besides these high grade branched so called heterogalactans, vasodilatoric and hypotensive macromolecules belonging to the substance class of glycoproteins are proven. Impaired immune defense, prostate adenoma.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For oral intake: 1 x 5-10 drops before a meal. For rubbing in: 1 x 5-10 drops at the location of the disease or into the bend of the elbow. In case of simultaneous treatment with injections, rub in 2 x weekly 5-10 drops on injection-free days. In cases of known hypersensitivity to Fomitopsis pinicola, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Fomepikehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X.

Duration of treatment: How supplied:

62

Fomepikehl 5X
Ampules
Liquid dilution for injection

Active ingredients: Composition:

Fomitopsis pinicola extract 5X 1 ampule of 1 ml contains: Medically active substance: 1 ml Fomitopsis pinicola 5X aqueous dilut. Other constituents: isotonic sodium chloride solution. According to the latest studies, polysaccarid extracts from Fomitopsis pinicola prove to be highly effective immune modulators. Besides these high grade branched so called heterogalactans, vasodilatoric and hypotensive macromolecules belonging to the substance class of glycoproteins are proven. Impaired immune defense, prostate adenoma.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intramuscularly or subcutaneously, 2 x weekly. In cases of known hypersensitivity to Fomitopsis pinicola, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Fomepikehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X.

Duration of treatment: How supplied:

63

Formasan 6X/12X/30X/200X
Drops
Liquid dilution for oral intake

Active ingredient: Composition:

Acidum formicicum 6X/12X/30X/200X 1 ml liquid dilution contains: Medically active substance: 0.25 ml Acidum formicicum 6X dil., 0.25 ml Acidum formicicum 12X dil., 0.25 ml Acidum formicicum 30X dil., 0.25 ml Acidum formicicum 200X dil. Other constituents: purified water, ethanol. The active ingredient of Formasan is formic acid, at all times an important therapeutic agent in folk medicine. The acid is produced from the forest ant Formica rufa. For generations, the alcoholic extract serves as embrocation in cases of arthrosis, arthritis and rheumatism. In the human body formic acid is a result of the protein metabolism. Eduard Krull (1842-1914), MD, observed that tuberculin patients didnt form any or not enough formic acid. Many tests to remedy the formic acid deficiency in tubercular patients led at the beginning of the 20th century to an effective ant-acid-therapy for the till then, little susceptible tuberculosis. Todays priority is the treatment of rheumatic diseases with allergic diathesis. In homeopathy, ant acid is a highly effective constitutional preparation for uric, rheumatic and allergic conditions. Rheumatism of the muscles and joints, eczema, bronchial asthma, allergies.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: In acute conditions 5-10 drops every half to one hour up to a maximum of 12 times per day. In chronic cases 1-3 x daily 5 drops before a meal. None known. None known.

Contraindications: Adverse reactions: Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

64

Advice: How supplied:

This preparation contains 50.6 % (v/v) alcohol (ethanol). The following dosage forms are available:100 ml dropper bottle 6X/12X/ 30X/200X potency mixture, 2 ml ampule 10 and 50 6X/12X/30X/200X potency mixture.

65

Formasan
Ampules

6X/12X/30X/200X

Liquid dilution for injection

Active ingredient: Composition:

Acidum formicicum 6X/12X/30X/200X 1 ampule of 2 ml contains: Medically active substance: 0.5 ml Acidum formicicum 6X aqueous dilut., 0.5 ml Acidum formicicum 12X aqueous dilut., 0.5 ml Acidum formicicum 30X aqueous dilut., 0.5 ml Acidum formicicum 200X aqueous dilut. Other constituents: isotonic sodium chloride solution. The active ingredient of Formasan is formic acid, at all times an important therapeutic agent in folk medicine. The acid is produced from the forest ant Formica rufa. For generations, the alcoholic extract serves as embrocation in cases of arthrosis, arthritis and rheumatism. In the human body formic acid is a result of the protein metabolism. Eduard Krull (1842-1914), MD, observed that tuberculin patients didnt form any or not enough formic acid. Many tests to remedy the formic acid deficiency in tubercular patients led at the beginning of the 20th century to an effective ant-acid-therapy for the till then, little susceptible tuberculosis. Todays priority is the treatment of rheumatic diseases with allergic diathesis. In homeopathy, ant acid is a highly effective constitutional preparation for uric, rheumatic and allergic conditions. Rheumatism of the muscles and joints, eczema, bronchial asthma, allergies.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 2 ml to be injected either intramuscularly or subcutaneously, 1-2 x weekly. None known. None known.

Contraindications: Adverse reactions: Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 100 ml dropper bottle 6X/12X/ 30X/200X potency mixture, 2 ml ampule 10 and 50 6X/12X/30X/200X potency mixture.

Duration of treatment: How supplied:

66

Fortakehl 5X
Drops
Liquid dilution for oral intake, rubbing in, inhalation

Active ingredient: Composition:

Penicillium roquefortii extract 5X 1 ml liquid dilution contains: Medically active substance: 1 ml Penicillium roquefortii 5X dil. Other constituents: purified water. Fortakehl is obtained from the mold fungus Penicillium roquefortii; it is not an antibiotic and does not produce antibiotic substances. Therefore, there is no occurrence of side effects that may occur during an antibiotic treatment, such as allergies, liver damage, destruction of the intestinal flora, and the formation of penicillin-resistant strains. Fortakehl is given at the beginning of symbiosis recovery treatment for all intestinal mycoses and, consecutively, for all other mycoses, such as those of the vaginal region, the skin and the mouth. According to Enderlein, the blood of humans and all mammals always contains the so-called Endobiont of a plant origin. The most primitive form of the Endobiont is the apathogenic colloidal stage, characterized by tiny protein particles in the size of viruses (0.01 m). A developmental cycle of primitive forms via the bacterial phase, up to the fungal stage is initiated by endogenic and exogenic factors whereby the virulence of the parasite increases with the rising developmental stage. There is no human being who has not acquired this Endobiont via the placenta and is not hosting at least the primitive stages in his cells and body fluids. In the healthy body, these primitive forms serve as regulators because they are able to mate with cyclogenetically higher parasite forms and to degrade them to lower stages. The body must then eliminate their debris from the body. When a complete elimination via skin, intestine, kidneys and bronchi is not possible another upward cycle may develop. To avoid this, the elimination or destruction needs to be supported by appropriate preparations. Promotion of symbiosis in dysbacteria and for destroyed mucosa (mucous membranes), gastritis, enteritis, colitis syndrome with cholecystitis and pancreatitis with the following complaints: diarrhea, constipation, vomitus, gastric ulcer, mycoses of the intestine, the vagina, and the skin. Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops before a meal. For rubbing in: 1 x daily 5-10 drops at the location of the disease or into the bend of the elbow. In case of simultaneous treatment with injections, rub in 2 x weekly 5-10 drops on injection-free days. For inhalation: 10-20 drops, inhaled deeply 2-3 x daily. In cases of known hypersensitivity to Penicillium roquefortii, as a precaution, this preparation should not be administered.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

67

Adverse reactions:

None known. Because of specific organic components of Fortakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment: Advice: How supplied:

Penicillium roquefortii as an active ingredient is also contained in Exmykehl.


The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X.

68

Fortakehl 5X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Penicillium roquefortii extract 5X 1 ampule of 1 ml contains: Medically active substance: 1 ml Penicillium roquefortii 5X aqueous dilut. Other constituents: isotonic sodium chloride solution. Fortakehl is obtained from the mold fungus Penicillium roquefortii; it is not an antibiotic and does not produce antibiotic substances. Therefore, there is no occurrence of side effects that may occur during an antibiotic treatment, such as allergies, liver damage, destruction of the intestinal flora, and the formation of penicillin-resistant strains. Fortakehl is given at the beginning of symbiosis recovery treatment for all intestinal mycoses and, consecutively, for all other mycoses, such as those of the vaginal region, the skin and the mouth. According to Enderlein, the blood of humans and all mammals always contains the so-called Endobiont of a plant origin. The most primitive form of the Endobiont is the apathogenic colloidal stage, characterized by tiny protein particles in the size of viruses (0.01 m). A developmental cycle of primitive forms via the bacterial phase, up to the fungal stage is initiated by endogenic and exogenic factors whereby the virulence of the parasite increases with the rising developmental stage. There is no human being who has not acquired this Endobiont via the placenta and is not hosting at least the primitive stages in his cells and body fluids. In the healthy body, these primitive forms serve as regulators because they are able to mate with cyclogenetically higher parasite forms and to degrade them to lower stages. The body must then eliminate their debris from the body. When a complete elimination via skin, intestine, kidneys and bronchi is not possible another upward cycle may develop. To avoid this, the elimination or destruction needs to be supported by appropriate preparations. Promotion of symbiosis in dysbacteria and for destroyed mucosa (mucous membranes), gastritis, enteritis, colitis syndrome with cholecystitis and pancreatitis with the following complaints: diarrhea, constipation, vomitus, gastric ulcer, mycoses of the intestine, the vagina, and the skin. Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intracutaneously or subcutaneously, 2 x weekly. In cases of known hypersensitivity to Penicillium roquefortii, as a precaution, this preparation should not be administered.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

69

Adverse reactions:

None known. Because of specific organic components of Fortakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment: Advice: How supplied:

Penicillium roquefortii as an active ingredient is also contained in Exmykehl.


The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X.

70

Fortakehl 6X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Penicillium roquefortii extract 6X 1 ampule of 1 ml contains: Medically active substance: 1 ml Penicillium roquefortii 6X aqueous dilut. Other constituents: isotonic sodium chloride solution. Fortakehl is obtained from the mold fungus Penicillium roquefortii; it is not an antibiotic and does not produce antibiotic substances. Therefore, there is no occurrence of side effects that may occur during an antibiotic treatment, such as allergies, liver damage, destruction of the intestinal flora, and the formation of penicillin-resistant strains. Fortakehl is given at the beginning of symbiosis recovery treatment for all intestinal mycoses and, consecutively, for all other mycoses, such as those of the vaginal region, the skin and the mouth. According to Enderlein, the blood of humans and all mammals always contains the so-called Endobiont of a plant origin. The most primitive form of the Endobiont is the apathogenic colloidal stage, characterized by tiny protein particles in the size of viruses (0.01 m). A developmental cycle of primitive forms via the bacterial phase, up to the fungal stage is initiated by endogenic and exogenic factors whereby the virulence of the parasite increases with the rising developmental stage. There is no human being who has not acquired this Endobiont via the placenta and is not hosting at least the primitive stages in his cells and body fluids. In the healthy body, these primitive forms serve as regulators because they are able to mate with cyclogenetically higher parasite forms and to degrade them to lower stages. The body must then eliminate their debris from the body. When a complete elimination via skin, intestine, kidneys and bronchi is not possible another upward cycle may develop. To avoid this, the elimination or destruction needs to be supported by appropriate preparations. Promotion of symbiosis in dysbacteria and for destroyed mucosa (mucous membranes), gastritis, enteritis, colitis syndrome with cholecystitis and pancreatitis with the following complaints: diarrhea, constipation, vomitus, gastric ulcer, mycoses of the intestine, the vagina, and the skin. Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intracutaneously or subcutaneously, 2 x weekly. In cases of known hypersensitivity to Penicillium roquefortii, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Fortakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

71

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment: Advice: How supplied:

Penicillium roquefortii as an active ingredient is also contained in Exmykehl.


The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X.

72

Fortakehl 5X
Tablets

Active ingredient: Composition:

Penicillium roquefortii extract 5X 1 tablet contains: Medically active substance: 250 mg Penicillium roquefortii 5X trit. Other constituents: lactose, potato starch, magnesium stearate. Fortakehl is obtained from the mold fungus Penicillium roquefortii; it is not an antibiotic and does not produce antibiotic substances. Therefore, there is no occurrence of side effects that may occur during an antibiotic treatment, such as allergies, liver damage, destruction of the intestinal flora, and the formation of penicillin-resistant strains. Fortakehl is given at the beginning of symbiosis recovery treatment for all intestinal mycoses and, consecutively, for all other mycoses, such as those of the vaginal region, the skin and the mouth. According to Enderlein, the blood of humans and all mammals always contains the so-called Endobiont of a plant origin. The most primitive form of the Endobiont is the apathogenic colloidal stage, characterized by tiny protein particles in the size of viruses (0.01 m). A developmental cycle of primitive forms via the bacterial phase, up to the fungal stage is initiated by endogenic and exogenic factors whereby the virulence of the parasite increases with the rising developmental stage. There is no human being who has not acquired this Endobiont via the placenta and is not hosting at least the primitive stages in his cells and body fluids. In the healthy body, these primitive forms serve as regulators because they are able to mate with cyclogenetically higher parasite forms and to degrade them to lower stages. The body must then eliminate their debris from the body. When a complete elimination via skin, intestine, kidneys and bronchi is not possible another upward cycle may develop. To avoid this, the elimination or destruction needs to be supported by appropriate preparations. Promotion of symbiosis in dysbacteria and for destroyed mucosa (mucous membranes), gastritis, enteritis, colitis syndrome with cholecystitis and pancreatitis with the following complaints: diarrhea, constipation, vomitus, gastric ulcer, mycoses of the intestine, the vagina, and the skin. Unless otherwise prescribed: 1-3 tablets daily taken with some liquid. In cases of known hypersensitivity to Penicillium roquefortii, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Fortakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application: Contraindications:

Adverse reactions:

73

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment: Advice: How supplied:

Penicillium roquefortii as an active ingredient is also contained in Exmykehl.


The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X.

74

Fortakehl 4X
Capsules
For oral intake

Active ingredient: Composition:

Penicillium roquefortii extract 4X 1 capsule contains: Medically active substance: 330 mg Penicillium roquefortii 4X trit. Other constituents: lactose, hypromellosis (capsule shell) Fortakehl is obtained from the mold fungus Penicillium roquefortii; it is not an antibiotic and does not produce antibiotic substances. Therefore, there is no occurrence of side effects that may occur during an antibiotic treatment, such as allergies, liver damage, destruction of the intestinal flora, and the formation of penicillin-resistant strains. Fortakehl is given at the beginning of symbiosis recovery treatment for all intestinal mycoses and, consecutively, for all other mycoses, such as those of the vaginal region, the skin and the mouth. According to Enderlein, the blood of humans and all mammals always contains the so-called Endobiont of a plant origin. The most primitive form of the Endobiont is the apathogenic colloidal stage, characterized by tiny protein particles in the size of viruses (0.01 m). A developmental cycle of primitive forms via the bacterial phase, up to the fungal stage is initiated by endogenic and exogenic factors whereby the virulence of the parasite increases with the rising developmental stage. There is no human being who has not acquired this Endobiont via the placenta and is not hosting at least the primitive stages in his cells and body fluids. In the healthy body, these primitive forms serve as regulators because they are able to mate with cyclogenetically higher parasite forms and to degrade them to lower stages. The body must then eliminate their debris from the body. When a complete elimination via skin, intestine, kidneys and bronchi is not possible another upward cycle may develop. To avoid this, the elimination or destruction needs to be supported by appropriate preparations. Promotion of symbiosis in dysbacteria and for destroyed mucosa (mucous membranes), gastritis, enteritis, colitis syndrome with cholecystitis and pancreatitis with the following complaints: diarrhea, obstipation, vomitus, gastric ulcer, mycoses of the intestine, the vagina, and the skin. Unless otherwise prescribed: 1-3 capsules daily taken with some liquid. In cases of known hypersensitivity to Penicillium roquefortii, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Fortakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application: Contraindications:

Adverse reactions:

75

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment: Advice: How supplied:

Penicillium roquefortii as an active ingredient is also contained in Exmykehl.


The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X.

76

Fortakehl 3X
Suppositories

Active ingredient: Composition:

Penicillium roquefortii extract 3X 1 suppository contains: Medically active substance: 0.2 g Penicillium roquefortii 3X trit. Other constituents: hard fat, lactose. Fortakehl is obtained from the mold fungus Penicillium roquefortii; it is not an antibiotic and does not produce antibiotic substances. Therefore, there is no occurrence of side effects that may occur during an antibiotic treatment, such as allergies, liver damage, destruction of the intestinal flora, and the formation of penicillin-resistant strains. Fortakehl is given at the beginning of symbiosis recovery treatment for all intestinal mycoses and, consecutively, for all other mycoses, such as those of the vaginal region, the skin and the mouth. According to Enderlein, the blood of humans and all mammals always contains the so-called Endobiont of a plant origin. The most primitive form of the Endobiont is the apathogenic colloidal stage, characterized by tiny protein particles in the size of viruses (0.01 m). A developmental cycle of primitive forms via the bacterial phase, up to the fungal stage is initiated by endogenic and exogenic factors whereby the virulence of the parasite increases with the rising developmental stage. There is no human being who has not acquired this Endobiont via the placenta and is not hosting at least the primitive stages in his cells and body fluids. In the healthy body, these primitive forms serve as regulators because they are able to mate with cyclogenetically higher parasite forms and to degrade them to lower stages. The body must then eliminate their debris from the body. When a complete elimination via skin, intestine, kidneys and bronchi is not possible another upward cycle may develop. To avoid this, the elimination or destruction needs to be supported by appropriate preparations. Promotion of symbiosis in dysbacteria and for destroyed mucosa (mucous membranes), gastritis, enteritis, colitis syndrome with cholecystitis and pancreatitis with the following complaints: diarrhea, constipation, vomitus, gastric ulcer, mycoses of the intestine, the vagina, and the skin, adnexitis, sterility. Unless otherwise prescribed: 1x daily, insert 1 suppository rectally at bedtime. In cases of known hypersensitivity to Penicillium roquefortii, as a precaution, this preparation should not be administered.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

77

Adverse reactions:

None known. Because of specific organic components of Fortakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment: Advice: How supplied:

Penicillium roquefortii as an active ingredient is also contained in Exmykehl.


The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X.

78

Ginkgobakehl 1X
Drops
Liquid dilution for oral intake

Active ingredient: Composition:

Ginkgo biloba extract mother tincture 1 ml liquid dilution contains: Medically active substance: 1 ml Ginkgo biloba e foliis sicc. 1X dil. Other constituents: purified water, ethanol. The Ginkgo tree (Ginkgo biloba) has lived on Earth for approximately 300 million years. The home of this ancient durable plant lies in Asia. The Chinese have used healing remedies from the Ginkgo tree since 3,000 B.C. with the expressed intent of mitigating complaints and diseases connected with aging. Circulatory disorders (arterial and peripheral), arteriosclerosis, weakness in concentration, tiredness.

Characteristics:

According to experience, to be administered in cases of: Application: Contraindications: Adverse reactions:

Unless otherwise prescribed: For oral intake: 3-5 x daily 10-15 drops. None known. None known. Because of specific organic components of Ginkgobakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The preparation contains 66 % (v/v) alcohol (ethanol). The following dosage forms are available: 30 ml dropper bottle 1X, 4X, 2 ml ampule 10 and 50 4X.

Duration of treatment: Advice: How supplied:

79

Ginkgobakehl 4X
Drops
Liquid dilution for oral intake

Active ingredient: Composition:

Ginkgo biloba extract 4X 1 ml liquid dilution contains: Medically active substance: 1 ml Ginkgo biloba e foliis sicc. 4X dil. Other constituents: purified water, ethanol. The Ginkgo tree (Ginkgo biloba) has lived on Earth for approximately 300 million years. The home of this ancient durable plant lies in Asia. The Chinese have used healing remedies from the Ginkgo tree since 3,000 B.C. with the expressed intent of mitigating complaints and diseases connected with aging. Circulatory disorders (arterial and peripheral), arteriosclerosis, weakness in concentration, tiredness.

Characteristics:

According to experience, to be administered in cases of: Application: Contraindications: Adverse reactions:

Unless otherwise prescribed: For oral intake: 3-5 x daily 10-15 drops. None known. None known. Because of specific organic components of Ginkgobakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The preparation contains 52 % (v/v) alcohol (ethanol). The following dosage forms are available: 30 ml dropper bottle 1X, 4X, 2 ml ampule 10 and 50 4X.

Duration of treatment: Advice: How supplied:

80

Ginkgobakehl 4X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Ginkgo biloba extract 4X 1 ampule of 2 ml contains: Medically active substance: 2 ml Ginkgo biloba e foliis sicc. 4X aqueous dilut. Other constituents: isotonic sodium chloride solution. The Ginkgo tree (Ginkgo biloba) has lived on Earth for approximately 300 million years. The home of this ancient durable plant lies in Asia. The Chinese have used healing remedies from the Ginkgo tree since 3000 B.C. with the expressed intent of mitigating complaints and diseases connected with aging. Circulatory disorders (arterial and peripheral), arteriosclerosis, weakness ness in concentration, tiredness.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 2 ml to be injected either intramuscularly, subcutaneously, intracutaneously or intravenously, 1-3 x weekly. None known. None known. Because of specific organic components of Ginkgobakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications: Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 30 ml dropper bottle 1X, 4X, 2 ml ampule 10 and 50 4X.

Duration of treatment: How supplied:

81

Grifokehl 5X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Grifola frondosa extract 5X 1 ml liquid solution contains: Medically active substance: 1 ml Grifola frondosa 5X dil. Other constituents: purified water. This remedy is produced from the aerial parts of the Grifola frondosa fungus (known as Maitake in Japan). It can be characterised as an adaptogen i.e. in that it has a compensatory effect independent from the cause of the disease. Investigations in Japan with cancer patients revealed a profuse deceleration in tumor growths with those receiving regular doses of Maitake, which is based on an enhanced cell mediated immune defense. This mechanism is also responsible for the antiviral activity of the fungus as well as reducing blood pressure and blood glucose. Adaptogenic effect on unbalanced body functions, for diabetes mellitus, hypertonia, obesity, immunostimulant.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For oral intake: 1x daily 5-10 drops before a meal. For rubbing in: 1x daily 5-10 drops at the location of the disease or into the bend of the elbow. In case of simultaneous treatment with injections, rub in 2x weekly 5-10 drops on injection-free days. In cases of known hypersensitivity to Grifola frondosa, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Grifokehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage form is available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X.

Duration of treatment: How supplied:

82

Grifokehl 5X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Grifola frondosa extract 5X 1 ml liquid solution contains: Medically active substance: 1 ml Grifola frondosa 5X aqueous dil. Other constituents: isotonic sodium chloride solution. This remedy is produced from the aerial parts of the Grifola frondosa fungus (known as Maitake in Japan). It can be characterised as an adaptogen i.e. in that it has a compensatory effect independent from the cause of the disease. Investigations in Japan with cancer patients revealed a profuse deceleration in tumor growths with those receiving regular doses of Maitake, which is based on an enhanced cell mediated immune defense. This mechanism is also responsible for the antiviral activity of the fungus as well as reducing blood pressure and blood glucose. Adaptogenic effect on unbalanced body functions, for diabetes mellitus, hypertonia, obesity, immunostimulant.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intramuscularly, subcutaneously, intracutaneously or intravenously, 2x weekly. In cases of known hypersensitivity to Grifola frondosa, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Grifokehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage form is available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X.

Duration of treatment: How supplied:

83

Hexacyl
Drops
For oral intake

Active ingredient:

sulphur 4X, lycopodium extract mother tincture, berberis extract mother tincture 10 g (corresponds to 10.99 ml) liquid dilution contains: Medically active substance: 3.00 g sulphur 4X dil, 0.10 g lycopodium mother tincture, 0.05 g berberis mother tincture. Other constituents: purified water, ethanol. The active ingredients of Hexacyl - sulphur, lycopodium and berberis - present a similar range of effectiveness in their homeopathic drug picture. Each of the individual substances show a priority in venous stasis symptoms in the circulatory system. Characteristic disturbances of other organs result from it, in particular the liver and kidneys. Main symptoms are: Severe burning and itching, exhaustion, deterioration with heat, cold and resting. Recovery with fresh air and moderate movement. Hexacyl is indicated for the elemination of all toxic or infectious damage with increased degradation of protein such as food intolerance, infections and intoxications. Supporting therapy by functional disorders of liver-gallbladder and kidneys.

Composition:

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: In acute cases: Every half hour to every hour (maximum 12 x daily) 5-10 drops with some water. In chronic cases: 13 x daily 5 drops with some water. None known. None known. Because of Hexacyls specific organic components, theoretically, hypersensitivity may occur. In this case, discontinue use and treat symptomatically.

Contraindications: Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

84

Duration of treatment: Advice: How supplied:

Dependent on the advice of the physician or health care professional. The preparation contains 59.9 % (v/v) alcohol (ethanol). The following dosage forms are available: 30 ml dropper bottle.

85

Larifikehl 5X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Laricifomes officinalis extract 5X 1 ml liquid dilution contains: Medically active substance: 1 ml Laricifomes officinalis e mycelio 5X dil. Other constituents: purified water. Larifikehl is a remedy produced from the Laricifomes officinalis fungus. In popular medicine, it has been used predominantly for night sweat in lung diseases, for asthma, cough, and also as a laxative. Larifikehl is produced from the mycelia of the tree-fungus in accordance with a process developed by Prof. Dr. G. Enderlein for the production of isopathic preparations from molds. Fever, lung diseases and inflammations of the digestive organs, for primary chronic polyarthritis.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For oral intake: 1x daily 5-10 drops before a meal. For rubbing in: 1x daily 5-10 drops at the location of the disease or into the bend of the elbow. In case of simultaneous treatment with injections, rub in 2x weekly 5-10 drops on injection-free days. In cases of known hypersensitivity to Laricifomes officinalis e mycelio, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Larifikehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 20 capsules 4X 10 suppositories 4X.

Duration of treatment: How supplied:

86

Larifikehl 5X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Laricifomes officinalis extract 5X 1 ampule of 1 ml contains: Medically active substance: 1 ml Laricifomes officinalis e mycelio 5X aqueous dilut. Other constituents: isotonic sodium chloride solution. Larifikehl is a remedy produced from the Laricifomes officinalis fungus. In popular medicine, it has been used predominantly for night sweat in lung diseases, for asthma, cough, as well as being a laxative. Larifikehl is produced from the mycelia of the tree-fungus in accordance with a process developed by Prof. G. Enderlein for the production of isopathic preparations from molds. Fever, lung diseases and inflammations of the digestive organs, for primary chronic polyarthritis.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intramuscularly, intravenously, subcutaneously or intracutaneously, 2x weekly. In cases of known hypersensitivity to Laricifomes officinalis e mycelio, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Larifikehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 20 capsules 4X, 10 suppositories 4X.

Duration of treatment: How supplied:

87

Larifikehl 4X
Capsules
For oral intake

Active ingredient: Composition:

Laricifomes officinalis extract 4X 1 capsule contains: Medically active substance: 330 mg Laricifomes officinalis e mycelio 4X trit. Other constituents: lactose, hypromellosis (capsule shell) Larifikehl is a remedy produced from the Laricifomes officinalis fungus. In popular medicine, it has been used predominantly for night sweat in lung diseases, for asthma, cough, as well as being a laxative. Larifikehl is produced from the mycelia of the tree-fungus in accordance with a process developed by Prof. G. Enderlein for the production of isopathic preparations from molds. Fever, lung diseases and inflammations of the digestive organs, for primary chronic polyarthritis.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1-3 capsules daily, either before breakfast or at bedtime, taken with some liquid. In cases of known hypersensitivity to Laricifomes officinalis e mycelio, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Larifikehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 20 capsules 4X, 10 suppositories 4X.

Duration of treatment: How supplied:

88

Larifikehl 4X
Suppositories

Active ingredient: Composition:

Laricifomes officinalis extract 4X 1 suppository contains: Medically active substance: 0.2 g Laricifomes officinalis e mycelio 4X trit. Other constituents: hard fat, lactose. Larifikehl is a remedy produced from the Laricifomes officinalis fungus. In popular medicine, it has been used predominantly for night sweat in lung diseases, for asthma, cough, as well as being a laxative. Larifikehl is produced from the mycelia of the tree-fungus in accordance with a process developed by Prof. G. Enderlein for the production of isopathic preparations from molds. Fever, lung diseases and inflammations of the digestive organs, for primary chronic polyarthritis.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally at bedtime. In cases of known hypersensitivity to Laricifomes officinalis e mycelio, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Larifikehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 4X, 20 capsules 4X.

Duration of treatment: How supplied:

89

Latensin 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Bacillus cereus extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Bacillus cereus 6X dil. Other constituents: purified water. Latensin is a preparation of the non-pathogenic Bacillus cereus. Due to its contents of protein substances, polysaccharides, and ferments, it brings about a distinctly activating effect of endogenic defense and healing functions in chronic inflammatory diseases. In immunological testing models, a high rise of granulocytic phagocytosis activity has been recorded. A strong increase in the T-lymphocyte proliferation also certifies Latensin as a potent immune modulator. Chronic inflammations in respiratory tract and intestines, chronic rheumatic and dermal diseases, for immune modulation.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For oral intake: 1-3 x daily 2-5 drops before a meal. For rubbing in: 2-3 x weekly 5-10 drops at the location of the disease or into the bend of the elbow. In cases of known hypersensitivity to Bacillus cereus, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Latensin, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

Duration of treatment: How supplied:

90

Latensin 4X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Bacillus cereus extract 4X 1 ampule of 1 ml contains: Medically active substance: 1 ml Bacillus cereus 4X aqueous dilut. Other constituents: isotonic sodium chloride solution. Latensin is a preparation of the non-pathogenic Bacillus cereus. Due to its contents of protein substances, polysaccharides, and ferments, it brings about a distinctly activating effect of endogenic defense and healing functions in chronic inflammatory diseases. In immunological testing models, a high rise of granulocytic phagocytosis activity has been recorded. A strong increase in the T-lymphocyte proliferation also certifies Latensin as a potent immune modulator. Chronic inflammations in respiratory tract and intestines, chronic rheumatic and dermal diseases, for immune modulation.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 1 ml to be injected deep intramuscularly (regular intragluteally) while the patient is lying down, every two weeks. Normally the treatment is started with the administration of capsules 6X or 4X or with injection 6X. In case of absent or weak reactions, the dosage may be gradually raised by shorter intervals - 2 ampules maximum per week. In case of strong reactions, injections have to be discontinued; the treatment can be continued with the dosage form capsules. As a general advice, the dosage must be adequately chosen so that strong general reactions do not occur and that local reactions are confined to the site of the injection. Fever, conditions of weakness. In cases of known hypersensitivity to Bacillus cereus, as a precaution, this preparation should not be administered. None known. Generally well tolerated. Occasionally local reactions like rubefaction, swelling or painfulness may be observed, normally vanishing without treatment. These effects are not to be seen as adverse reactions, but rather as an expression of effectiveness. In the first 2 or 3 days after the injection sometimes conditions of weakness, fortified expectoration, slight painfulness of the region or subfebrile temperatures may occur. Strong general reactions are always a sign of overdosage or of incorrect injection technique. In this case the treatment can be continued orally with Latensin capsules 6X or 4X. None known. An interval of four weeks should be kept to the administration of vaccinations. In cases of simultaneous treatment with immunosuppressive remedies, the effectiveness of Latensin may be influenced.

Contraindications:

Adverse reactions:

Interactions with other remedies:

91

Side effects: Precautions:

None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. Latensin is an excellent therapeutic agent of the so-called paratuberculosis and all diseases accompanied by tuberculation. The therapy should always be started with the weakest concentration. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

Duration of treatment: Advice:

How supplied:

92

Latensin 6X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Bacillus cereus extract 6X 1 ampule of 1 ml contains: Medically active substance: 1 ml Bacillus cereus 6X aqueous dilut. Other constituents: isotonic sodium chloride solution. Latensin is a preparation of the non-pathogenic Bacillus cereus. Due to its contents of protein substances, polysaccharides, and ferments, it brings about a distinctly activating effect of endogenic defense and healing functions in chronic inflammatory diseases. In immunological testing models, a high rise of granulocytic phagocytosis activity has been recorded. A strong increase in the T-lymphocyte proliferation also certifies Latensin as a potent immune modulator. Chronic inflammations in respiratory tract and intestines, chronic rheumatic and dermal diseases, for immune modulation.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 1 ml to be injected deep intramuscularly (regular intragluteally) while the patient is lying down, every two weeks. Normally the treatment is started with the administration of capsules 6X or 4X. In case of absent or weak reactions the dosage may be gradually raised by shorter intervals - 2 ampules weekly at the most - and/ or by the injection of strength 4X. In case of strong reactions, injections have to be discontinued; the treatment can be continued with the dosage form capsules. As a general advice, the dosage has to be chosen adequately, so that strong general reactions do not occur and the local reactions are confined to the site of injections. Fever, conditions of weakness. In cases of known hypersensitivity to Bacillus cereus, as a precaution, this preparation should not be administered. None known. Generally well tolerated. Occasionally local reactions like rubefaction, swelling or painfulness may be observed, normally vanishing without treatment. These effects are not to be seen as adverse reactions, but rather as an expression of effectiveness. In the first 2 or 3 days after the injection sometimes conditions of weakness, fortified expectoration, slight painfulness of the region or subfebrile temperatures may occur. Strong general reactions are always a sign of overdosage or of incorrect injection technique. In this case the treatment can be continued orally with Latensin capsules 6X or 4X. None known. An interval of four weeks should be kept to the administration of vaccinations. In cases of simultaneous treatment with immunosuppressive remedies, the effectiveness of Latensin may be influenced.

Contraindications:

Adverse reactions:

Interactions with other remedies:

93

Side effects: Precautions:

None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. Latensin is an excellent therapeutic agent of the so-called paratuberculosis and all diseases accompanied by tuberculation. The therapy should always be started with the weakest concentration. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

Duration of treatment: Advice:

How supplied:

94

Latensin 4X
Capsules
For oral intake

Active ingredient: Composition:

Bacillus cereus extract 4X 1 capsule contains: Medically active substance: 330 mg Bacillus cereus 4X trit. Other constituents: lactose, hypromellosis (capsule shell). Latensin is a preparation of the non-pathogenic Bacillus cereus. Due to its contents of protein substances, polysaccharides, and ferments, it brings about a distinctly activating effect of endogenic defense and healing functions in chronic inflammatory diseases. In immunological testing models, a high rise of granulocytic phagocytosis activity has been recorded. A strong increase in the T-lymphocyte proliferation also certifies Latensin as a potent immune modulator. Chronic inflammations in respiratory tract and intestines, chronic rheumatic and dermal diseases, for immune modulation.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1-2x weekly 1 capsule at bedtime, taken with some liquid. In cases of known hypersensitivity to Bacillus cereus, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Latensin, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. Under the noticeable stimulus threshold, a good effect of Latensin is guaranteed. Latensin is an excellent therapeutic agent of the so-called paratuberculosis and all diseases accompanied by tuberculation. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

Duration of treatment: Advice:

How supplied:

95

Latensin 6X
Capsules
For oral intake

Active ingredient: Composition:

Bacillus cereus extract 6X 1 capsule contains: Medically active substance: 330 mg Bacillus cereus 6X trit. Other constituents: lactose, hypromellosis (capsule shell). Latensin is a preparation of the non-pathogenic Bacillus cereus. Due to its contents of protein substances, polysaccharides, and ferments, it brings about a distinctly activating effect of endogenic defense and healing functions in chronic inflammatory diseases. In immunological testing models, a high rise of granulocytic phagocytosis activity has been recorded. A strong increase in the T-lymphocyte proliferation also certifies Latensin as a potent immune modulator. Chronic inflammations in respiratory tract and intestines, chronic rheumatic and dermal diseases, for immune modulation.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1-2x weekly 1 capsule at bedtime, taken with some liquid. In cases of known hypersensitivity to Bacillus cereus, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Latensin, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. Under the noticeable stimulus threshold, a good effect of Latensin is guaranteed. Latensin is an excellent therapeutic agent of the so-called paratuberculosis and all diseases accompanied by tuberculation. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

Duration of treatment: Advice:

How supplied:

96

Latensin 6X
Suppositories

Active ingredient: Composition:

Bacillus cereus extract 6X 1 suppository contains: Medically active substance: 0.2 g Bacillus cereus 6X trit. Other constituents: hard fat, lactose Latensin is a preparation of the non-pathogenic Bacillus cereus. Due to its contents of protein substances, polysaccharides, and ferments, it brings about a distinctly activating effect of endogenic defense and healing functions in chronic inflammatory diseases. In immunological testing models, a high rise of granulocytic phagocytosis activity has been recorded. A strong increase in the T-lymphocyte proliferation also certifies Latensin as a potent immune modulator. Chronic inflammations in respiratory tract and intestines, chronic rheumatic and dermal diseases, for immune modulation.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 - 3 x weekly 1 suppository, inserted into the rectum at bedtime. In cases of known hypersensitivity to Bacillus cereus, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Latensin, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

Duration of treatment: How supplied:

97

Leptospermusan 1X
Drops
Liquid dilution for oral intake

Active ingredient: Composition:

Leptospermum scoparium extract 1X 1 ml liquid dilution contains: Medically active substance: 1 ml Leptospermum scoparium 1X dil. Other constituents: purified water, ethanol

Characteristics:

Leptospermum scoparium or manuka is a wild growing bush found in New Zealand and is well known in Polynesian folk medicine. Preparations from its leaves, bark and seed pods were used for treating different diseases, but especially for dysentery and diarrhoea. As with other species of the myrtles, Leptospermum scoparium contains etheric oils, well known for their antibacterial activity. The anthelmintic property of Leptospermum was also reported. Further pharmacological effective constituents are tannins as well as rare flavonoids.
Secondary effects of apoplexy, ischaemic attack, inflammations such as trigeminal neuralgia, iritis, allergic conjunctivitis, diseases of the respiratory tract such as cold and sore throat, for a general soothing influence, gastrointestinal diseases such as gastritis, pylorospasm, constipation, colitis. Unless otherwise prescribed: For oral intake: 1-3 x daily 5 drops. None known. None known. Because of specific organic components of Leptospermusan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

According to experience, to be administered in cases of:

Application: Contraindications: Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The preparation contains 70 % (v/v) alcohol (ethanol). The following dosage forms are available: 30 ml dropper bottle 1X.

Duration of treatment: Advice: How supplied:

98

Leptucin 6X
Capsules
For oral intake

Active ingredient: Composition:

Propionibacterium avidum extract 6X 1 capsule contains: Medically active substance: 330 mg Propionibacterium avidum 6X trit. Other constituents: lactose, hypromellosis (capsule shell)

Characteristics:

Propionibacteria belong to the strongest immunomodulators. Due to the special structure of their cell wall they are able to stimulate the immune system by activation of the monocyte-macrophage-system. They have antibacterial, antiviral, antiparasitic, and antitumor properties. Leptucin contains the cell walls of the strain Propionibacterium avidum KP 40. In tests on the unspecific immunostimulation the homeopathically prepared cell wall fraction revealed interesting effects dependent on the applied decimal potency. In these studies, a strong immunostimulation was not seen under a 5X dilution. Moreover, Leptucin is a potent remedy for stimulation of the circulatory system especially in the head and extremities.
Immunostimulation, stimulation of the circulation of the extremities, vascular migraine, tinnitus, inflammation of the urinary bladder.

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1-3 capsules per week at bedtime, taken with some liquid. In cases of known hypersensitivity to Propionibacterium avidum, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Leptucin, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 5 capsules 6X, 10 suppositories 6X.

Duration of treatment: How supplied:

99

Leptucin 6X
Suppositories

Active ingredient: Composition:

Propionibacterium avidum extract 6X 1 suppository contains: Medically active substance: 0.2 g Propionibacterium avidum 6X trit. Other constituents: hard fat, lactose.

Characteristics:

Propionibacteria belong to the strongest immunomodulators. Due to the special structure of their cell wall they are able to stimulate the immune system by activation of the monocyte-macrophage-system. They have antibacterial, antiviral, antiparasitic, and antitumor proper ties. Leptucin contains the cell walls of the strain Propionibacterium avidum KP 40. In tests on the unspecific immunostimulation the homeopathically prepared cell wall fraction revealed interesting effects dependent on the applied decimal potency. In these studies, a strong immunostimulation was not seen under a 5X dilution. Moreover, Leptucin is a potent remedy for stimulation of the circulatory system especially in the head and extremities.
Immunostimulation, stimulation of the circulation of the extremities, vascular migraine, tinnitus, inflammation of the urinary bladder.

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1-3x weekly, insert 1 suppository rectally at bedtime. In cases of known hypersensitivity to Propionibacterium avidum, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Leptucin, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 5 capsules 6X, 10 suppositories 6X.

Duration of treatment: How supplied:

100

Lipiscor
Capsules
For oral intake

Active ingredient: Composition:

Polyunsaturated fatty acids (PUFA) 1 capsule contains: Medically active substance: 500 mg fatty acids (from sea fish), containing 70 mg icosapent and 50 mg doconexent. Other constituents: d--tocopherol, dl--tocopherolum aceticum, gelatin, glycerol, purified water. Lipiscor contains natural fish oil with a high content of essential unsaturated omega-3-(n-3) fatty acids, which is icosapent (eicosapentaenoic acid) and doconexent (docosahexaenoic acids). The results of epidemiological studies on populations such as Innuits, Japanese, Dutch and Americans show a correlation between a high intake of deep-sea fish and a low appearance of cardiovascular diseases. The regular intake of Lipiscor leads to a lowering of plasma triglycerides within four weeks. If taken on a permanent basis the triglyceride level will remain constant. If discontinued, the plasma triglycerides will return to their former level within 2-3 month. The omega-3-fatty acids that are contained in Lipiscor, are absorbed into the normal lipid metabolism, particularly the metabolism of eicosanoid and prostaglandin. The lipid-lowering effect of Lipiscor is probably the result of an inhibition of the triglyceride-synthesis. Taking Lipiscor increases the proportion of n-3 (omega-3) fatty acids. To lower a highly increased triacylglycerol blood level. In addition Lipiscor should only be administered if a diet is insufficient in lowering the triglyceride level. Unless otherwise prescribed: 5-10 capsules twice daily. Lipiscor is to be swallowed whole with some liquid before a meal. Acute and subacute pancreatitis, acute pancreatic necrosis, acute and chronic liver intoxications, cirrhosis of the liver of various origin, acute to chronic cholecystitis, suppuration of the gallbladder, disorders of the digestion and emulsification of fat in the small intestine due to disease of the gallbladder and/or pancreas, thrombopathia, during pregnancy and in case of hypercholesterinaemia a thorough consideration of benefit and risk is required. None known. Since Lipiscor prolongs the bleeding time and may reduce the platelet aggregation, patients with thrombopathia and patients who are treated with anticoagulant drugs, should be under constant medical supervision as it might be necessary to reduce the administration of anticoagulant drugs.

Characteristics:

Indication:

Application:

Contraindications:

Adverse reactions: Interactions with other remedies:

101

Side effects:

High dosages may occasionally cause nausea and eructation. Lipiscor may prolong bleeding time as well as inhibit the platelet aggregation. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 60 capsules

Precautions:

Duration of treatment: How supplied:

102

Luffasan 4X
Drops
For oral intake

Active ingredient: Composition:

Luffa operculata extract 4X 1 ml liquid dilution contains: Medically active substance: 1 ml Luffa operculata 4X dil. Other constituents: purified water, ethanol. Luffasan is produced from the ripe, dried fruits of Luffa operculata (related to the pumpkin family) and is a universal remedy in Brazils folk medicine for constipation, oedemas and tumours. Luffasan is predominantly used as a decongestant in cases of blockages caused by inflammation. Hay fever, cold, headache, dyspepsia.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: In acute cases: Every half hour to every hour (maximum 12 x daily) 5 drops. In chronic cases: 1-3 x daily 5 drops. None known. None known. Because of specific organic components of Luffasan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications: Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The preparation contains 52 % (v/v) alcohol (ethanol). The following dosage forms are available: 10ml dropper bottle 4X, 80 tablets 4X.

Duration of treatment: Advice: How supplied:

103

Luffasan 4X
Tablets

Active ingredient: Composition:

Luffa operculata extract 4X 1 tablet contains: Medically active substance: 250 mg Luffa operculata 4X trit. Other constituents: lactose, potato starch, magnesium stearate. Luffasan is produced from the ripe, dried fruits of Luffa operculata (related to the pumpkin family) and is a universal remedy in Brazils folk medicine for constipation, oedemas and tumours. Luffasan is predominantly used as a decongestant in cases of blockages caused by inflammation. Hay fever, cold, headache, dyspepsia.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: In acute cases: Every half hour to every hour (maximum 12 x daily) 1 tablet. In chronic cases: 1-3 x daily 1 tablet. None known. None known. Because of specific organic components of Luffasan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications: Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10ml dropper bottle 4X, 80 tablets 4X.

Duration of treatment: How supplied:

104

Mapurit
Capsules
For oral intake

Active ingredient: Composition:

DL--tocopheryl acetate, magnesium oxide 1 capsule contains: 200 mg DL--tocopheryl acetate (vitamin-E acetate), 250 mg magnesium oxide. Other constituents: soybean oil, soybean lecithin, coconut fat, palm nut oil, yellow beeswax, gelatin, glycerol, sorbitol, purified water, titanium dioxide, yellow iron oxide, chlorophyllin-sodium/copper Mapurit improves all disorders of the nervous system (muscle cramps, paresthesia, disorders of concentration, quick psychical and physical exhaustion, dyspnoea), of the gastrointestinal tract (alternating constipation and diarrhea, colicky spasm) of the cardiovascular system (tachycardia and arrhythmia, angina pectoris, vascular constriction as well as increased sensitivity against digitalis), of the female genital system (late menarche, disorders of the cycle, dysmenorrhoea, hypermenorrhoea) as well as of the nutritional state (disturbance signs as onychoschisis and increased cariogenicity) positively which are caused by hypomagnesaemia. Vitamin E with -tocopherol, a fat soluble vitamin, whose main function is its antioxidant effect in metabolism. Vitamin E in large quantities accumulates in the lipid layer of the cell membrane and protects against oxidative damages. This effect, which stabilizes the mitochondria, is the therapeutic base of vitamin E in cases of oxygen deficiency, angiocardiopathy, symptoms of old age, in high-performance sports and in cases of mental and physical stress situations. For improvement of vitality, Vitamin-E-deficiency in cases of disturbed absorption if a parenteral administration of vitamin E is not necessary; hypomagnesemia: if it is the cause for disorders of the muscular activity (neuromuscular disorders; calf cramps) Unless otherwise prescribed: adolescents and adults take 1 capsule with some liquid in the morning and evening. In case of renal insufficiency and arrhythmia the remedy should not be taken without medical supervision. If possible, check the electrolyte state to assure that there is no contraindication. None known. Magnesium preparations should not betaken simultaneously with tetracycline bacuase of the mutual disturbance of resorption. The iron resorption may be disturbed through the intake of magnesium.

Characteristics:

Indications:

Application:

Contraindications:

Adverse reactions: Interactions with other remedies:

105

Side effects:

In case of high dosages, loose stool may result which, however, is harmless. In case of a large dosage and long continuous intake of the preparation tiredness may appear. This may be an indication that an increased magnesium concentration has already been reached in the blood. For safety reasons the intake should then be discontinued. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Vitality deficiency and other diseases which result from vitamin E or magnesium deficiency often have other causes. If the intake is unsuccessful a clinical diagnosis should be made in case of serious complaints. Dependent on the advice of the physician or health care professional. Package with 50 capsules, multiple package with 10 x 50 capsules.

Precautions:

Advice:

Duration of treatment: How supplied:

106

Mucedokehl 5X
Drops
Liquid dilution for oral intake, rubbing in, inhalation

Active ingredient: Composition:

Mucor mucedo extract 5X 1 ml liquid dilution contains: Medically active substance: 1 ml Mucor mucedo 5X dil. Other constituents: purified water. This preparation produced from Mucor mucedo, a mold fungus, shows a strong preference to the head area in its field of effectiveness. Mucedokehl is a preparation from the different sexual mycelial types of Mucor mucedo. In pharmacology, there are also substances with right and left turning characteristics which display different physiological effects. Mucedokehl combines components of strains which sexually differentiate themselves, leading to a living bi-polarity within the preparation, thus providing a new, expanded spectrum of effectiveness. Neuro-vegetative syndrome (anxiety), regulatory dysfunctions in the lymphatic system, chronic respiratory diseases, sinusitis, tonsillitis, sinobronchitis, ostitis, lymphostasis, thyroid function disorders. Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops before a meal. For rubbing in: 1 x daily 5-10 drops at the location of the disease or into the bend of the elbow. In case of simultaneous treatment with injections, rub in 2 x weekly 5-10 drops on injection-free days. For inhalation: 10-20 drops, inhaled deeply 2-3 x daily. In cases of known hypersensitivity to Mucor mucedo, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Mucedokehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

Duration of treatment: How supplied:

107

Mucedokehl 5X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Mucor mucedo extract 5X 1 ampule of 1 ml contains: Medically active substance: 1 ml Mucor mucedo 5X aqueous dilut. Other constituents: isotonic sodium chloride solution. This preparation produced from Mucor mucedo, a mold fungus, shows a strong preference to the head area in its field of effectiveness. Mucedokehl is a preparation from the different sexual mycelial types of Mucor mucedo. In pharmacology, there are also substances with right and left turning characteristics which display different physiological effects. Mucedokehl combines components of strains which sexually differentiate themselves, leading to a living bi-polarity within the preparation, thus providing a new, expanded spectrum of effectiveness. Neuro-vegetative syndrome (anxiety), regulatory dysfunctions in the lymphatic system, chronic respiratory diseases, sinusitis, tonsillitis, sinobronchitis, ostitis, lymphostasis, thyroid function disorders. Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intramuscularly, subcutaneously, intracutaneously or intravenously, 2 x weekly. In cases of known hypersensitivity to Mucor mucedo, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Mucedokehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

Duration of treatment: How supplied:

108

Mucedokehl 4X
Capsules
For oral intake

Active ingredient: Composition:

Mucor mucedo extract 4X 1 capsule contains: Medically active substance: 330 mg Mucor mucedo 4X trit. Other constituents: lactose, hypromellosis (capsule shell). This preparation produced from Mucor mucedo, a mold fungus, shows a strong preference to the head area in its field of effectiveness. Mucedokehl is a preparation from the different sexual mycelial types of Mucor mucedo. In pharmacology, there are also substances with right and left turning characteristics which display different physiological effects. Mucedokehl combines components of strains which sexually differentiate themselves, leading to a living bi-polarity within the preparation, thus providing a new, expanded spectrum of effectiveness. Neuro-vegetative syndrome (anxiety), regulatory dysfunctions in the lymphatic system, chronic respiratory diseases, sinusitis, tonsillitis, sinobronchitis, ostitis, lymphostasis, thyroid function disorders. Unless otherwise prescribed: 1-3 capsules daily taken with some liquid. In cases of known hypersensitivity to Mucor mucedo, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Mucedokehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application: Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

Duration of treatment: How supplied:

109

Mucedokehl 3X
Suppositories

Active ingredient: Composition:

Mucor mucedo extract 3X 1 suppository contains: Medically active substance: 0.2 g Mucor mucedo 3X trit. Other constituents: hard fat, lactose. This preparation produced from Mucor mucedo, a mold fungus, shows a strong preference to the head area in its field of effectiveness. Mucedokehl is a preparation from the different sexual mycelial types of Mucor mucedo. In pharmacology, there are also substances with right and left turning characteristics which display different physiological effects. Mucedokehl combines components of strains which sexually differentiate themselves, leading to a living bi-polarity within the preparation, thus providing a new, expanded spectrum of effectiveness. Neuro-vegetative syndrome (anxiety), regulatory dysfunctions in the lymphatic system, chronic respiratory diseases, sinusitis, tonsillitis, sinobronchitis, ostitis, lymphostasis, thyroid function disorders. Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally at bedtime. In cases of known hypersensitivity to Mucor mucedo, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Mucedokehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X

Duration of treatment: How supplied:

110

Mucokehl 5X
Drops
Liquid dilution for oral intake, rubbing in, inhalation

Active ingredient: Composition:

Mucor racemosus extract 5X 1 ml liquid dilution contains: Medically active substance: 1 ml Mucor racemosus 5X dil. Other constituents: purified water. In the blood and tissue of humans and animals, live microbes which are responsible for maintaining diverse regulatory mechanisms and are normally harmless. According to Prof. Enderlein, these Endobionts are usually non-pathogenic phases of the Mucor racemosus mold fungus. As with all microbes, they are subject to the law of cyclogeny i.e. their development progresses in the following stages: primitive phase - bacterium - fungus, whereby the endobionts virulence and pathogenicity increases with the rising developmental phase. If one supplies a diseased organism stricken with higher valences with certain lower valences, then these are able to degrade the pathogenic forms into the inactive primitive stage. They can then be eliminated through the urinary path, intestine, skin and bronchi. Chronic, latent and acute infirmities of the vascular system, such as thromboses, embolism, post-infarct processes, angina pectoris, circulatory disorders and disturbed healing of wounds, such as smokers leg, diabetic gangrene, venous diseases, such as varicosity, hemorrhoids, glaucoma, cataract and as a start-up for a symbiosis therapy. Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops before a meal. For rubbing in: 1 x daily 5-10 drops at the location of the disease or into the bend of the elbow. In case of simultaneous treatment with injections, rub in 2 x weekly 5-10 drops on injection-free days. For inhalation: 10-20 drops, inhaled deeply 2-3 x daily. In cases of known hypersensitivity to Mucor racemosus, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Mucokehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

Do not administer simultaneously with Notakehl. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

111

Duration of treatment: Advice:

Dependent on the advice of the physician or health care professional. In isopathic therapy, Mucokehl is administered in the treatment of all blood diseases and vascular system diseases or disorders with their causes lying in congestions, blockages and blocked energy flow. The active ingredient of Mucokehl is also part of the Sankombi combination preparation. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X.

How supplied:

112

Mucokehl 5X
Eye drops
Liquid dilution for the eyes

Active ingredient: Composition:

Mucor racemosus extract 5X 1 ml liquid dilution contains: Medically active substance: 999.95 mg Mucor racemosus 5X dil. Other constituents: isotonic sodium chloride solution, 0.05 mg chlorohexidinediacetate. In the blood and tissue of humans and animals, live microbes which are responsible for maintaining diverse regulatory mechanisms and are normally harmless. According to Prof. Enderlein, these Endobionts are usually nonpathogenic phases of the Mucor racemosus mold fungus. As with all microbes, they are subject to the law of cyclogeny i.e. their development progresses in the following stages: primitive phase - bacterium - fungus, whereby the endobionts virulence and pathogenicity increases with the rising developmental phase. If one supplies a diseased organism stricken with higher valences with certain lower valences, then these are able to degrade the pathogenic forms into the inactive primitive stage. They can then be eliminated through the urinary path, intestine, skin and bronchi. Glaucoma, cataract, scintillating scotoma, conjunctivitis.

Characteristics:

According to experience, to be administered in cases of: Application: Contraindications:

Unless otherwise prescribed: Drip 1 drop twice daily into the affected eye. In cases of known hypersensitivity to Mucor racemosus, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Mucokehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

Do not administer simultaneously with Notakehl. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

113

Advice:

In isopathic therapy, Mucokehl is administered in the treatment of all blood diseases and vascular system diseases or disorders with their causes lying in congestions, blockages and blocked energy flow. The active ingredient of Mucokehl is also part of the Sankombi combination preparation. After opening, use within one month. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X.

How supplied:

114

Mucokehl 5X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Mucor racemosus extract 5X 1 ampule of 1 ml contains: Medically active substance: 1 ml Mucor racemosus 5X aqueous dilut. Other constituents: isotonic sodium chloride solution. In the blood and tissue of humans and animals, live microbes which are responsible for maintaining diverse regulatory mechanisms and are normally harmless. According to Prof. Enderlein, these Endobionts are usually nonpathogenic phases of the Mucor racemosus mold fungus. As with all microbes, they are subject to the law of cyclogeny i.e. their development progresses in the following stages: primitive phase - bacterium - fungus, whereby the endobionts virulence and pathogenicity increases with the rising developmental phase. If one supplies a diseased organism stricken with higher valences with certain lower valences, then these are able to degrade the pathogenic forms into the inactive primitive stage. They can then be eliminated through the urinary path, intestine, skin and bronchi. Chronic, latent and acute infirmities of the vascular system, such as thromboses, embolism, post-infarct processes, angina pectoris, circulatory disorders and disturbed healing of wounds, such as smokers leg, diabetic gangrene, venous diseases, such as varicosity, hemorrhoids, glaucoma, cataract and as a start-up for a symbiosis therapy. Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intramuscularly, subcutaneously, intracutaneously or intravenously, 2 x weekly. In cases of known hypersensitivity to Mucor racemosus, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Mucokehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

Do not administer simultaneously with Notakehl. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

115

Advice:

In isopathic therapy, Mucokehl is administered in the treatment of all blood diseases and vascular system diseases or disorders with their causes lying in congestions, blockages and blocked energy flow. The active ingredient of Mucokehl is also part of the Sankombi combination preparation. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X.

How supplied:

116

Mucokehl 6X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Mucor racemosus extract 6X 1 ampule of 1 ml contains: Medically active substance: 1 ml Mucor racemosus 6X aqueous dilut. Other constituents: isotonic sodium chloride solution. In the blood and tissue of humans and animals, live microbes which are responsible for maintaining diverse regulatory mechanisms and are normally harmless. According to Prof. Enderlein, these Endobionts are usually nonpathogenic phases of the Mucor racemosus mold fungus. As with all microbes, they are subject to the law of cyclogeny i.e. their development progresses in the following stages: primitive phase - bacterium - fungus, whereby the endobionts virulence and pathogenicity increases with the rising developmental phase. If one supplies a diseased organism stricken with higher valences with certain lower valences, then these are able to degrade the pathogenic forms into the inactive primitive stage. They can then be eliminated through the urinary path, intestine, skin and bronchi. Chronic, latent and acute infirmities of the vascular system, such as thromboses, embolism, post-infarct processes, angina pectoris, circulatory disorders and disturbed healing of wounds, such as smokers leg, diabetic gangrene, venous diseases, such as varicosity, hemorrhoids, glaucoma, cataract and as a start-up for a symbiosis therapy. Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intramuscularly, subcutaneously, intracutaneously or intravenously, 2 x weekly. In cases of known hypersensitivity to Mucor racemosus, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Mucokehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

Do not administer simultaneously with Notakehl. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

117

Advice:

In isopathic therapy, Mucokehl is administered in the treatment of all blood diseases and vascular system diseases or disorders with their causes lying in congestions, blockages and blocked energy flow. The active ingredient of Mucokehl is also part of the Sankombi combination preparation. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X.

How supplied:

118

Mucokehl 7X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Mucor racemosus extract 7X 1 ampule of 1 ml contains: Medically active substance: 1 ml Mucor racemosus 7X aqueous dilut. Other constituents: isotonic sodium chloride solution. In the blood and tissue of humans and animals, live microbes which are responsible for maintaining diverse regulatory mechanisms and are normally harmless. According to Prof. Enderlein, these Endobionts are usually nonpathogenic phases of the Mucor racemosus mold fungus. As with all microbes, they are subject to the law of cyclogeny i.e. their development progresses in the following stages: primitive phase - bacterium - fungus, whereby the endobionts virulence and pathogenicity increases with the rising developmental phase. If one supplies a diseased organism stricken with higher valences with certain lower valences, then these are able to degrade the pathogenic forms into the inactive primitive stage. They can then be eliminated through the urinary path, intestine, skin and bronchi. Chronic, latent and acute infirmities of the vascular system, such as thromboses, embolism, post-infarct processes, angina pectoris, circulatory disorders and disturbed healing of wounds, such as smokers leg, diabetic gangrene, venous diseases, such as varicosity, hemorrhoids, glaucoma, cataract and as a start-up for a symbiosis therapy. Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intramuscularly, subcutaneously, intracutaneously or intravenously, 2 x weekly. In cases of known hypersensitivity to Mucor racemosus, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Mucokehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

Do not administer simultaneously with Notakehl. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

119

Advice:

In isopathic therapy, Mucokehl is administered in the treatment of all blood diseases and vascular system diseases or disorders with their causes lying in congestions, blockages and blocked energy flow. The active ingredient of Mucokehl is also part of the Sankombi combination preparation. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X.

How supplied:

120

Mucokehl 5X
Tablets

Active ingredient: Composition:

Mucor racemosus extract 5X 1 tablet contains: Medically active substance: 250 mg Mucor racemosus 5X trit. Other constituents: lactose, potato starch, magnesium stearate. In the blood and tissue of humans and animals, live microbes which are responsible for maintaining diverse regulatory mechanisms and are normally harmless. According to Prof. Enderlein, these Endobionts are usually nonpathogenic phases of the Mucor racemosus mold fungus. As with all microbes, they are subject to the law of cyclogeny i.e. their development progresses in the following stages: primitive phase - bacterium - fungus, whereby the endobionts virulence and pathogenicity increases with the rising developmental phase. If one supplies a diseased organism stricken with higher valences with certain lower valences, then these are able to degrade the pathogenic forms into the inactive primitive stage. They can then be eliminated through the urinary path, intestine, skin and bronchi. Chronic, latent and acute infirmities of the vascular system, such as thromboses, embolism, post-infarct processes, angina pectoris, circulatory disorders and disturbed healing of wounds, such as smokers leg, diabetic gangrene, venous diseases, such as varicosity, hemorrhoids, glaucoma, cataract and as a start-up for a symbiosis therapy. Unless otherwise prescribed: 1-3 tablets daily taken with some liquid. In cases of known hypersensitivity to Mucor racemosus, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Mucokehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application: Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

Do not administer simultaneously with Notakehl. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

121

Advice:

In isopathic therapy, Mucokehl is administered in the treatment of all blood diseases and vascular system diseases or disorders with their causes lying in congestions, blockages and blocked energy flow. The active ingredient of Mucokehl is also part of the Sankombi combination preparation. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X.

How supplied:

122

Mucokehl 4X
Capsules
For oral intake

Active ingredient: Composition:

Mucor racemosus extract 4X 1 capsule contains: Medically active substance: 330 mg Mucor racemosus 4X trit. Other constituents: lactose, hypromellosis (capsule shell). In the blood and tissue of humans and animals, live microbes which are responsible for maintaining diverse regulatory mechanisms and are normally harmless. According to Prof. Enderlein, these Endobionts are usually nonpathogenic phases of the Mucor racemosus mold fungus. As with all microbes, they are subject to the law of cyclogeny i.e. their development progresses in the following stages: primitive phase - bacterium - fungus, whereby the endobionts virulence and pathogenicity increases with the rising developmental phase. If one supplies a diseased organism stricken with higher valences with certain lower valences, then these are able to degrade the pathogenic forms into the inactive primitive stage. They can then be eliminated through the urinary path, intestine, skin and bronchi. Chronic, latent and acute infirmities of the vascular system, such as thromboses, embolism, post-infarct processes, angina pectoris, circulatory disorders and disturbed healing of wounds, such as smokers leg, diabetic gangrene, venous diseases, such as varicosity, hemorrhoids, glaucoma, cataract and as a start-up for a symbiosis therapy. Unless otherwise prescribed: 1-3 capsules daily, either before breakfast or at bedtime, taken with some liquid. In cases of known hypersensitivity to Mucor racemosus, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Mucokehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

Do not administer simultaneously with Notakehl. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

123

Advice:

In isopathic therapy, Mucokehl is administered in the treatment of all blood diseases and vascular system diseases or disorders with their causes lying in congestions, blockages and blocked energy flow. The active ingredient of Mucokehl is also part of the Sankombi combination preparation. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X.

How supplied:

124

Mucokehl 3X
Suppositories

Active ingredient: Composition:

Mucor racemosus extract 3X 1 suppository contains: Medically active substance: 0.2 g Mucor racemosus 3X trit. Other constituents: hard fat, lactose. In the blood and tissue of humans and animals, live microbes which are responsible for maintaining diverse regulatory mechanisms and are normally harmless. According to Prof. Enderlein, these Endobionts are usually nonpathogenic phases of the Mucor racemosus mold fungus. As with all microbes, they are subject to the law of cyclogeny i.e. their development progresses in the following stages: primitive phase - bacterium - fungus, whereby the endobionts virulence and pathogenicity increases with the rising developmental phase. If one supplies a diseased organism stricken with higher valences with certain lower valences, then these are able to degrade the pathogenic forms into the inactive primitive stage. They can then be eliminated through the urinary path, intestine, skin and bronchi. Circulatory disorders, smokers leg, embolism, thrombosis, hemorrhoids, anal fissures, inflammatory diseases of organs in the small pelvis, such as endometritis, prostatitis, ovarian- and tubal cysts, sterility, adenoma of the prostate, rectal carcinoma, colitis syndrome, diverticulitis, lymphostasis. Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally at bedtime. In cases of known hypersensitivity to Mucor racemosus, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Mucokehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

Do not administer simultaneously with Notakehl. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

125

Advice:

In isopathic therapy, Mucokehl is administered in the treatment of all blood diseases and vascular system diseases or disorders with their causes lying in congestions, blockages and blocked energy flow. The active ingredient of Mucokehl is also part of the Sankombi combination preparation. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X.

How supplied:

126

Mucokehl 3X
Ointment

Active ingredient: Composition:

Mucor racemosus extract 3X 1 g ointment contains: Medically active substance: 0.1 g Mucor racemosus 3X dil. Other constituents: 0.38 g Lanolin alcohol ointment, 0.1 g Coconut oil fract., 0.03 g Glyceryl monostearate 40-50%, 0.23 g Propylene glycol, 0.02 g Magnesium sulphate x 7 H2O, 0.01g Lactic acid, 0.13 g water for injection. In the blood and tissue of humans and animals, live microbes which are responsible for maintaining diverse regulatory mechanisms and are normally harmless. According to Prof. Enderlein, these Endobionts are usually nonpathogenic phases of the Mucor racemosus mold fungus. As with all microbes, they are subject to the law of cyclogeny i.e. their development progresses in the following stages: primitive phase - bacterium - fungus, whereby the endobionts virulence and pathogenicity increases with the rising developmental phase. If one supplies a diseased organism stricken with higher valences with certain lower valences, then these are able to degrade the pathogenic forms into the inactive primitive stage. They can then be eliminated through the urinary path, intestine, skin and bronchi. Diseases of the veins and their disturbed circulation as varicosis, thrombophlebitis, hemorrhoids, generally for inflammatory diseases, swellings, contusions, distortions, ischialgia, cicatricial keloids, chronic dermatitis. Unless otherwise prescribed: Apply on the affected area 1 to 3 x daily. In cases of known hypersensitivity to Mucor racemosus, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Mucokehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application: Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

Do not administer simultaneously with Notakehl. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

127

Advice:

In isopathic therapy, Mucokehl is administered in the treatment of all blood diseases and vascular system diseases or disorders with their causes lying in congestions, blockages and blocked energy flow. The active ingredient of Mucokehl is also part of the Sankombi combination preparation. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X, 30 g tube of ointment 3X, 5 ml eye drops 5X.

How supplied:

128

Mucokehl Atox 6X (Excretion)


Drops
Liquid dilution for oral intake, rubbing in
Active ingredient: Composition: Mucor racemosus antichondrit serum 6X 1 ml liquid dilution contains: Medically active substance: 1 ml rabbit serum 6X dil., derived from rabbits that were pre-treated with Mucor racemosus 3X dil. Other constituents: purified water. Mucokehl Atox 6X is a highly effective preparation in supporting and eliminating metabolic and decomposition products, especially after application with Mucokehl. Every effective biological therapy leads to an increase of degradation products and toxins which frequently fail to be eliminated due to blockages and congestive conditions. Because this could worsen a disease, elimination is the basic requirement for an effective therapy. Elimination after application of Mucokehl.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops before a meal. For rubbing in: 1 x daily 5-10 drops at the location of the disease or into the bend of the elbow. None known. None known.

Contraindications: Adverse reactions: Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. To be administered 1 day after Mucokehl at the earliest. Drink plenty of fluids. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 6X.

Duration of treatment: Advice:

How supplied:

129

Mucokehl Atox 6X (Excretion)


Ampules
Liquid dilution for injection
Active ingredient: Composition: Mucor racemosus antichondrit serum 6X 1 ampule of 1 ml contains: Medically active substance: 1 ml rabbit serum 6X aqueous dilut., derived from rabbits that were pre-treated with Mucor racemosus 3X dil. Other constituents: isotonic sodium chloride solution. Mucokehl Atox 6X is a highly effective preparation in supporting and eliminating metabolic and decomposition products, especially after application with Mucokehl. Every effective biological therapy leads to an increase of degradation products and toxins which frequently fail to be eliminated due to blockages and congestive conditions. Because this could worsen a disease, elimination is the basic requirement for an effective therapy. Elimination after application of Mucokehl.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intramuscularly, intracutaneously or subcutaneously, 2 x weekly. None known. None known.

Contraindications: Adverse reactions: Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. To be administered 1 day after Mucokehl at the earliest. Drink plenty of fluids. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 6X.

Duration of treatment: Advice:

How supplied:

130

Muscarsan 6X
Drops
Liquid dilution for oral intake

Active ingredient: Composition:

Amanita muscaria extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Amanita muscaria 6X dil. Other constituents: purified water, ethanol. The Amanita muscaria fungus is known for its characteristic appearance and toxicity. From its biological active ingredients, Muscarin has been well known the longest. The ancient nordic folk used the fungus to stimulate their battle lust. Even today, sibirian nomads use it as an intoxicant. The occuring symptoms after consumption of the dried fungus are similar to those known as with drug abuse. Today, Amanita muscaria is only applied for therapeutic purposes in homeopathy as the range of application is relatively broad. The main ones are cerebral and nervous overexcitement and exhaustion conditions, headache with pupils or students, cerebral circulatory disorders, vertigo, intoxicated and ecstatic conditions, manic psychoses, delirium tremens, muscular and organic spasms, migraine and vascular spasms. Nervous disorders of the intestinal tract, pain in the stomach from any cause, meteorism, chronic fermentative dyspepsia, damage from coffee and tabacco, alcoholism, drug and tablet abuse. Detoxification in case of drug and medication abuse, cerebral ischaemic attack; nervous and cerebral hyperexcitability, spasms of muscles, organs and blood vessels, migraine, nervous disorders of the intestine. Unless otherwise prescribed: For oral intake: In case of acute conditions: 5 drops every half to one hour. For chronic forms: 1-3 x daily 5 drops. In cases of known hypersensitivity to Amanita muscaria, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Muscarsan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

131

Advice: How supplied:

The preparation contains 50 % (v/v) alcohol (ethanol). The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 80 tablets 6X.

132

Muscarsan 6X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Amanita muscaria extract 6X 1 ml liquid dilution contains: 1 ml Amanita muscaria 6X dil. Other constituents: isotonic sodium chloride solution. The Amanita muscaria fungus is known for its characteristic appearance and toxicity. From its biological active ingredients, Muscarin has been well known the longest. The ancient nordic folk used the fungus to stimulate their battle lust. Even today, sibirian nomads use it as an intoxicant. The occuring symptoms after consumption of the dried fungus are similar to those known as with drug abuse. Today, Amanita muscaria is only applied for therapeutic purposes in homeopathy as the range of application is relatively broad. The main ones are cerebral and nervous overexcitement and exhaustion conditions, headache with pupils or students, cerebral circulatory disorders, vertigo, intoxicated and ecstatic conditions, manic psychoses, delirium tremens, muscular and organic spasms, migraine and vascular spasms. Nervous disorders of the intestinal tract, pain in the stomach from any cause, meteorism, chronic fermentative dyspepsia, damage from coffee and tabacco, alcoholism, drug and tablet abuse. Detoxification in case of drug and medication abuse, cerebral ischaemic attack; nervous and cerebral hyperexcitability, spasms of muscles, organs and blood vessels, migraine, nervous disorders of the intestine. Unless otherwise prescribed: Daily 1-2 ml to be injected subcutaneously or intramuscularly. In cases of known hypersensitivity to Amanita muscaria, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Muscarsan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects:

None known. None known.

133

Precautions:

As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 80 tablets 6X.

Duration of treatment: How supplied:

134

Muscarsan 6X
Tablets

Active ingredient: Composition:

Amanita muscaria extract 6X 1 tablet contains: Medically active substance: 250 mg Amanita muscaria 6X trit. Other constituents: lactose, potato starch, magnesium stearate. The Amanita muscaria fungus is known for its characteristic appearance and toxicity. From its biological active ingredients, Muscarin has been well known the longest. The ancient nordic folk used the fungus to stimulate their battle lust. Even today, sibirian nomads use it as an intoxicant. The occuring symptoms after consumption of the dried fungus are similar to those known as with drug abuse. Today, Amanita muscaria is only applied for therapeutic purposes in homeopathy as the range of application is relatively broad. The main ones are cerebral and nervous overexcitement and exhaustion conditions, headache with pupils or students, cerebral circulatory disturbance, vertigo, intoxicated and ecstatic conditions, manic psychoses, delirium tremens, muscular and orgasnic spasms, migraine and vascular spasms. Nervous disorders of the intestinal tract, pain in the stomach from any cause, meteorism, chronic fermentative dyspepsia, damage from coffee and tabacco, alcoholism, drug and tablet abuse. Detoxification in case of drug and medication abuse, cerebral ischaemic attack; nervous and cerebral hyperexcitability, spasms of muscles, organs and blood vessels, migraine, nervous disorders of the intestine. Unless otherwise prescribed: children: 2 x daily -1 tablet, adults: 2 - 3 x daily - 1 tablet. In cases of known hypersensitivity to Amanita muscaria, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Muscarsan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

135

Duration of treatment: How supplied:

Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 80 tablets 6X.

136

Nigersan 5X
Drops
Liquid dilution for oral intake, rubbing in, inhalation

Active ingredient: Composition:

Aspergillus niger extract 5X 1 ml liquid dilution contains: Medically active substance: 1 ml Aspergillus niger 5X dil. Other constituents: purified water. Nigersan is a specific acting preparation in the isopathic and immunobiological treatment of paratuberculosis and its secondary diseases. In contrast to chemical, bacteriostatic or antibiotic preparations, Nigersan does not directly attack the tubercle bacillus, using instead (based on Enderleins teaching on bacteria-cyclogeny) a weak area in the cyclic development of the parasite in order to artificially accelerate a process, which spontaneously occurs under normal physiological conditions within the changing generations, especially in all healing processes. By a therapy with Nigersan, the tubercle bacillus is broken down from its parasitic form and phase into apathogenic forms which can then be eliminated through the intestine, bladder, skin, and bronchi. Diseases of the urogenital tract, including myoma, cysts, inflammations conditioned by paratuberculosis, such as Scheuermann disease, Perthes disease and Bechterew disease, osteochondrosis, lymphatism, goiter diseases, obesity, verrucae (warts). Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops before a meal. For rubbing in: 1 x daily 5-10 drops at the location of the disease or into the bend of the elbow. In case of simultaneous treatment with injections, rub in 2 x weekly 5-10 drops on injection-free days. For inhalation: 10-20 drops, inhaled deeply 2-3 x daily. In cases of known hypersensitivity to Aspergillus niger, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Nigersan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

137

Duration of treatment: Advice:

Dependent on the advice of the physician or health care professional. In isopathic therapy, Nigersan is administered for all paratubercular diseases. The alternating administration of Utilin or Utilin S with Nigersan, intensifies the action of Nigersan. Aspergillus niger is also an active ingredient of the Sankombi combination preparation. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X.

How supplied:

138

Nigersan 5X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Aspergillus niger extract 5X 1 ampule of 1 ml contains: Medically active substance: 1 ml Aspergillus niger 5X aqueous dilut. Other constituents: isotonic sodium chloride solution. Nigersan is a specific acting preparation in the isopathic and immunobiological treatment of paratuberculosis and its secondary diseases. In contrast to chemical, bacteriostatic or antibiotic preparations, Nigersan does not directly attack the tubercle bacillus, using instead (based on Enderleins teaching on bacteria-cyclogeny) a weak area in the cyclic development of the parasite in order to artificially accelerate a process, which spontaneously occurs under normal physiological conditions within the changing generations, especially in all healing processes. By a therapy with Nigersan, the tubercle bacillus is broken down from its parasitic form and phase into apathogenic forms which can then be eliminated through the intestine, bladder, skin, and bronchi. Diseases of the urogenital tract, including myoma, cysts, inflammations conditioned by paratuberculosis, such as Scheuermann disease, Perthes disease and Bechterew disease, osteochondrosis, lymphatism, goiter diseases, obesity, verrucae (warts). Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intramuscularly, subcutaneously, intracutaneously or intravenously, 2 x weekly. In cases of known hypersensitivity to Aspergillus niger, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Nigersan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

139

Advice:

In isopathic therapy, Nigersan is administered for all paratubercular diseases. The alternating administration of Utilin or Utilin S with Nigersan, intensifies the action of Nigersan. Aspergillus niger is also an active ingredient of the Sankombi combination preparation. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X.

How supplied:

140

Nigersan 6X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Aspergillus niger extract 6X 1 ampule of 1 ml contains: Medically active substance: 1 ml Aspergillus niger 6X aqueous dilut. Other constituents: isotonic sodium chloride solution. Nigersan is a specific acting preparation in the isopathic and immunobiological treatment of paratuberculosis and its secondary diseases. In contrast to chemical, bacteriostatic or antibiotic preparations, Nigersan does not directly attack the tubercle bacillus, using instead (based on Enderleins teaching on bacteria-cyclogeny) a weak area in the cyclic development of the parasite in order to artificially accelerate a process, which spontaneously occurs under normal physiological conditions within the changing generations, especially in all healing processes. By a therapy with Nigersan, the tubercle bacillus is broken down from its parasitic form and phase into apathogenic forms which can then be eliminated through the intestine, bladder, skin, and bronchi. Diseases of the urogenital tract, including myoma, cysts, inflammations conditioned by paratuberculosis, such as Scheuermann disease, Perthes disease and Bechterew disease, osteochondrosis, lymphatism, goiter diseases, obesity, verrucae (warts). Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intramuscularly, subcutaneously, intracutaneously or intravenously, 2 x weekly. In cases of known hypersensitivity to Aspergillus niger, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Nigersan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

141

Advice:

In isopathic therapy, Nigersan is administered for all paratubercular diseases. The alternating administration of Utilin or Utilin S with Nigersan, intensifies the action of Nigersan. Aspergillus niger is also an active ingredient of the Sankombi combination preparation. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X.

How supplied:

142

Nigersan 7X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Aspergillus niger extract 7X 1 ampule of 1 ml contains: Medically active substance: 1 ml Aspergillus niger 7X aqueous dilut. Other constituents: isotonic sodium chloride solution. Nigersan is a specific acting preparation in the isopathic and immunobiological treatment of paratuberculosis and its secondary diseases. In contrast to chemical, bacteriostatic or antibiotic preparations, Nigersan does not directly attack the tubercle bacillus, using instead (based on Enderleins teaching on bacteria-cyclogeny) a weak area in the cyclic development of the parasite in order to artificially accelerate a process, which spontaneously occurs under normal physiological conditions within the changing generations, especially in all healing processes. By a therapy with Nigersan, the tubercle bacillus is broken down from its parasitic form and phase into apathogenic forms which can then be eliminated through the intestine, bladder, skin, and bronchi. Diseases of the urogenital tract, including myoma, cysts, inflammations conditioned by paratuberculosis, such as Scheuermann disease, Perthes disease and Bechterew disease, osteochondrosis, lymphatism, goiter diseases, obesity, verrucae (warts). Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intramuscularly, subcutaneously, intracutaneously or intravenously, 2 x weekly. In cases of known hypersensitivity to Aspergillus niger, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Nigersan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

143

Advice:

In isopathic therapy, Nigersan is administered for all paratubercular diseases. The alternating administration of Utilin or Utilin S with Nigersan, intensifies the action of Nigersan. Aspergillus niger is also an active ingredient of the Sankombi combination preparation. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X.

How supplied:

144

Nigersan 5X
Tablets

Active ingredient: Composition:

Aspergillus niger extract 5X 1 tablet contains: Medically active substance: 250 mg Aspergillus niger 5X trit. Other constituents: lactose, potato starch, magnesium stearate. Nigersan is a specific acting preparation in the isopathic and immunobiological treatment of paratuberculosis and its secondary diseases. In contrast to chemical, bacteriostatic or antibiotic preparations, Nigersan does not directly attack the tubercle bacillus, using instead (based on Enderleins teaching on bacteria-cyclogeny) a weak area in the cyclic development of the parasite in order to artificially accelerate a process, which spontaneously occurs under normal physiological conditions within the changing generations, especially in all healing processes. By a therapy with Nigersan, the tubercle bacillus is broken down from its parasitic form and phase into apathogenic forms which can then be eliminated through the intestine, bladder, skin, and bronchi. Diseases of the urogenital tract, including myoma, cysts, inflammations conditioned by paratuberculosis, such as Scheuermann disease, Perthes disease and Bechterew disease, osteochondrosis, lymphatism, goiter diseases, obesity, verrucae (warts). Unless otherwise prescribed: 1-3 tablets daily taken with some liquid. In cases of known hypersensitivity to Aspergillus niger, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Nigersan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application: Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

145

Advice:

In isopathic therapy, Nigersan is administered for all paratubercular diseases. The alternating administration of Utilin or Utilin S with Nigersan, intensifies the action of Nigersan. Aspergillus niger is also an active ingredient of the Sankombi combination preparation. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X.

How supplied:

146

Nigersan 4X
Capsules
For oral intake

Active ingredient: Composition:

Aspergillus niger extract 4X 1 capsule contains: Medically active substance: 330 mg Aspergillus niger 4X trit. Other constituents: lactose, hypromellosis (capsule shell). Nigersan is a specific acting preparation in the isopathic and immunobiological treatment of paratuberculosis and its secondary diseases. In contrast to chemical, bacteriostatic or antibiotic preparations, Nigersan does not directly attack the tubercle bacillus, using instead (based on Enderleins teaching on bacteria-cyclogeny) a weak area in the cyclic development of the parasite in order to artificially accelerate a process, which spontaneously occurs under normal physiological conditions within the changing generations, especially in all healing processes. By a therapy with Nigersan, the tubercle bacillus is broken down from its parasitic form and phase into apathogenic forms which can then be eliminated through the intestine, bladder, skin, and bronchi. Diseases of the urogenital tract, including myoma, cysts, inflammations conditioned by paratuberculosis, such as Scheuermann disease, Perthes disease and Bechterew disease, osteochondrosis, lymphatism, goiter diseases, obesity, verrucae (warts). Unless otherwise prescribed: 1-3 capsules daily taken with some liquid. In cases of known hypersensitivity to Aspergillus niger, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Nigersan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application: Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

147

Advice:

In isopathic therapy, Nigersan is administered for all paratubercular diseases. The alternating administration of Utilin or Utilin S with Nigersan, intensifies the action of Nigersan. Aspergillus niger is also an active ingredient of the Sankombi combination preparation. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X.

How supplied:

148

Nigersan 3X
Suppositories

Active ingredient: Composition:

Aspergillus niger extract 3X 1 suppository contains: Medically active substance: 0.2 g Aspergillus niger 3X trit. Other constituents: hard fat, lactose. Nigersan is a specific acting preparation in the isopathic and immunobiological treatment of paratuberculosis and its secondary diseases. In contrast to chemical, bacteriostatic or antibiotic preparations, Nigersan does not directly attack the tubercle bacillus, using instead (based on Enderleins teaching on bacteria-cyclogeny) a weak area in the cyclic development of the parasite in order to artificially accelerate a process, which spontaneously occurs under normal physiological conditions within the changing generations, especially in all healing processes. By a therapy with Nigersan, the tubercle bacillus is broken down from its parasitic form and phase into apathogenic forms which can then be eliminated through the intestine, bladder, skin, and bronchi. Diseases of the urogenital tract, including epididymitis, adenoma of the prostate, ovarian cysts, inflammatory diseases of the large intestine such such as colitis syndrome, Crohns disease, ulcerative colitis, paratuberculously conditioned inflammations such as Scheuermann disease, Perthes disease and Bechterew disease, osteochondrosis, lymphatism, goiter diseases, obesity Unless otherwise prescribed: 1x daily, insert 1 suppository rectally at bedtime. In cases of known hypersensitivity to Aspergillus niger, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Nigersan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

149

Advice:

In isopathic therapy, Nigersan is administered for all paratubercular diseases. The alternating administration of Utilin or Utilin S with Nigersan, intensifies the action of Nigersan. Aspergillus niger is also an active ingredient of the Sankombi combination preparation. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X.

How supplied:

150

Nigersan Atox 6X (Excretion)


Drops
Liquid dilution for oral intake, rubbing in
Active ingredients: Composition: Aspergillus niger antichondrit serum 6X 1 ml liquid dilution contains: Medically active substance: 1 ml rabbit serum 6X dil., derived from rabbits that were pre-treated with Aspergillus niger 3X dil. Other constituents: purified water. Nigersan Atox 6X is a highly effective preparation in supporting and eliminating metabolic and decomposition products, especially after application of Nigersan. Every effective biological therapy leads to an increase of degradation products and toxins which frequently fail to be eliminated due to blockages and congestive conditions. Because this could worsen a disease, elimination is the basic condition for an effective therapy. For elimination after application of Nigersan.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops before a meal. For rubbing in: 1 x daily 5-10 drops at the location of the disease or into the bend of the elbow. None known. None known.

Contraindications: Adverse reactions: Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. To be administered 1 day after Nigersan at the earliest. Drink plenty of fluids. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 6X.

Duration of treatment: Advice:

How supplied:

151

Nigersan Atox 6X (Excretion)


Ampules
Liquid dilution for injection
Active ingredient: Composition: Aspergillus niger antichondrit serum 6X 1 ampule of 1 ml contains: Medically active substance: 1 ml rabbit serum 6X aqueous dilut., derived from rabbits that were pre-treated with Aspergillus niger 3X dil. Other constituents: isotonic sodium chloride solution. Nigersan Atox 6X is a highly effective preparation in supporting and eliminating metabolic and decomposition products, especially after application of Nigersan. Every effective biological therapy leads to an increase of degradation products and toxins which frequently fail to be eliminated due to blockages and congestive conditions. Because this could worsen a disease, elimination is the basic condition for an effective therapy. For elimination after application of Nigersan.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intramuscularly, intracutaneously or subcutaneously, 2 x weekly. None known. None known.

Contraindications: Adverse reactions: Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. To be administered 1 day after Nigersan at the earliest. Drink plenty of fluids. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 6X.

Duration of treatment: Advice:

How supplied:

152

Notakehl 5X
Drops
Liquid dilution for oral intake, rubbing in, inhalation

Active ingredient: Composition:

Penicillium chrysogenum extract 5X 1 ml liquid dilution contains: Medically active substance: 1 ml Penicillium chrysogenum 5X dil. Other constituents: purified water. Notakehl is produced from the Penicillium chrysogenum mold fungus. It is not an antibiotic and does not produce antibiotic substances, therefore, there are no side effects which may occur during a treatment with antibiotics, such as allergies, liver damages, destruction of intestinal flora and the formation of Penicillin resistant strains. Notakehl specifically acts with all infections caused by streptococci and staphylococci. With alternating applications of Mucokehl or Nigersan, Notakehl plays an important role for irritative therapy. It is not only useful in cases of unsatisfactory healing processes but also with serial applications of Mucokehl during the injections intervals, to administer Notakehl or Quentakehl in any preferred dosage form. For all general bacterial suppurations, e.g. angina tonsillitis, laryngitis; follow-up treatment for suppurations caused after tooth extractions, consecutive spinal conditions e.g. cervical spine, lumbal syndrome, otitis, neuritis, neuralgia; conditions of the urogenital system e.g. adenoma of the prostate, urinary tract infections, pulmonary diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis and acne. Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops before a meal. For rubbing in: 1 x daily 5-10 drops at the location of the disease or into the bend of the elbow. In case of simultaneous treatment with injections, rub in 2 x weekly 5-10 drops on injection-free days. For inhalation: 10-20 drops, inhaled deeply 2-3 x daily. In cases of known hypersensitivity to Penicillium chrysogenum, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Notakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

Do not administer simultaneously with Mucokehl. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

153

Duration of treatment: Advice:

Dependent on the advice of the physician or health care professional. Notakehl is used in isopathic therapy for all acute and chronic diseases caused by streptococcal or staphylococcal infections. Apply Notakehl as an interposition with herpes zoster; changing after one week to Quentakehl. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X, 30 g tube of ointment 3X.

How supplied:

154

Notakehl 5X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Penicillium chrysogenum extract 5X 1 ampule of 1 ml contains: Medically active substance: 1 ml Penicillium chrysogenum 5X aqueous dilut. Other constituents: isotonic sodium chloride solution. Notakehl is produced from the Penicillium chrysogenum mold fungus. It is not an antibiotic and does not produce antibiotic substances, therefore, there are no side effects which may occur during a treatment with antibiotics, such as allergies, liver damages, destruction of intestinal flora and the formation of Penicillin resistant strains. Notakehl specifically acts with all infections caused by streptococci and staphylococci. With alternating applications of Mucokehl or Nigersan, Notakehl plays an important role for irritative therapy. It is not only useful in cases of unsatisfactory healing processes but also with serial applications of Mucokehl during the injections intervals, to administer Notakehl or Quentakehl in any preferred dosage form. For all general bacterial suppurations, e.g. angina tonsillitis, laryngitis; follow-up treatment for suppurations caused after tooth extractions, consecutive spinal conditions e.g. cervical spine, lumbal syndrome, otitis, neuritis, neuralgia; conditions of the urogenital system e.g. adenoma of the prostate, urinary tract infections, pulmonary diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis and acne. Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intramuscularly, subcutaneously, intracutaneously or intravenously, 2 x weekly. In cases of known hypersensitivity to Penicillium chrysogenum, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Notakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

Do not administer simultaneously with Mucokehl. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

155

Advice:

Notakehl is used in isopathic therapy for all acute and chronic diseases caused by streptococcal or staphylococcal infections. Apply Notakehl as an interposition with herpes zoster; changing after one week to Quentakehl. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X, 30 g tube of ointment 3X.

How supplied:

156

Notakehl 6X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Penicillium chrysogenum extract 6X 1 ampule of 1 ml contains: Medically active substance: 1 ml Penicillium chrysogenum 6X aqueous dilut. Other constituents: isotonic sodium chloride solution. Notakehl is produced from the Penicillium chrysogenum mold fungus. It is not an antibiotic and does not produce antibiotic substances, therefore, there are no side effects which may occur during a treatment with antibiotics, such as allergies, liver damages, destruction of intestinal flora and the formation of Penicillin resistant strains. Notakehl specifically acts with all infections caused by streptococci and staphylococci. With alternating applications of Mucokehl or Nigersan, Notakehl plays an important role for irritative therapy. It is not only useful in cases of unsatisfactory healing processes but also with serial applications of Mucokehl during the injections intervals, to administer Notakehl or Quentakehl in any preferred dosage form. For all general bacterial suppurations, e.g. angina tonsillitis, laryngitis; follow-up treatment for suppurations caused after tooth extractions, consecutive spinal conditions e.g. cervical spine, lumbal syndrome, otitis, neuritis, neuralgia; conditions of the urogenital system e.g. adenoma of the prostate, urinary tract infections, pulmonary diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis and acne. Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intramuscularly, subcutaneously, intracutaneously or intravenously, 2 x weekly. In cases of known hypersensitivity to Penicillium chrysogenum, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Notakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

Do not administer simultaneously with Mucokehl. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

157

Advice:

Notakehl is used in isopathic therapy for all acute and chronic diseases caused by streptococcal or staphylococcal infections. Apply Notakehl as an interposition with herpes zoster; changing after one week to Quentakehl. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X, 30 g tube of ointment 3X.

How supplied:

158

Notakehl 7X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Penicillium chrysogenum extract 7X 1 ampule of 1 ml contains: Medically active substance: 1 ml Penicillium chrysogenum 7X aqueous dilut. Other constituents: isotonic sodium chloride solution. Notakehl is produced from the Penicillium chrysogenum mold fungus. It is not an antibiotic and does not produce antibiotic substances, therefore, there are no side effects which may occur during a treatment with antibiotics, such as allergies, liver damages, destruction of intestinal flora and the formation of Penicillin resistant strains. Notakehl specifically acts with all infections caused by streptococci and staphylococci. With alternating applications of Mucokehl or Nigersan, Notakehl plays an important role for irritative therapy. It is not only useful in cases of unsatisfactory healing processes but also with serial applications of Mucokehl during the injections intervals, to administer Notakehl or Quentakehl in any preferred dosage form. For all general bacterial suppurations, e.g. angina tonsillitis, laryngitis; follow-up treatment for suppurations caused after tooth extractions, consecutive spinal conditions e.g. cervical spine, lumbal syndrome, otitis, neuritis, neuralgia; conditions of the urogenital system e.g. adenoma of the prostate, urinary tract infections, pulmonary diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis and acne. Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intramuscularly, subcutaneously, intracutaneously or intravenously, 2 x weekly. In cases of known hypersensitivity to Penicillium chrysogenum, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Notakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

Do not administer simultaneously with Mucokehl. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

159

Advice:

Notakehl is used in isopathic therapy for all acute and chronic diseases caused by streptococcal or staphylococcal infections. Apply Notakehl as an interposition with herpes zoster; changing after one week to Quentakehl. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X, 30 g tube of ointment 3X.

How supplied:

160

Notakehl 5X
Tablets

Active ingredient: Composition:

Penicillium chrysogenum extract 5X 1 tablet contains: Medically active substance: 250 mg Penicillium chrysogenum 5X trit. Other constituents: lactose, potato starch, magnesium stearate. Notakehl is produced from the Penicillium chrysogenum mold fungus. It is not an antibiotic and does not produce antibiotic substances, therefore, there are no side effects which may occur during a treatment with antibiotics, such as allergies, liver damages, destruction of intestinal flora and the formation of Penicillin resistant strains. Notakehl specifically acts with all infections caused by streptococci and staphylococci. With alternating applications of Mucokehl or Nigersan, Notakehl plays an important role for irritative therapy. It is not only useful in cases of unsatisfactory healing processes but also with serial applications of Mucokehl during the injections intervals, to administer Notakehl or Quentakehl in any preferred dosage form. For all general bacterial suppurations, e.g. angina tonsillitis, laryngitis; follow-up treatment for suppurations caused after tooth extractions, consecutive spinal conditions e.g. cervical spine, lumbal syndrome, otitis, neuritis, neuralgia; conditions of the urogenital system e.g. adenoma of the prostate, urinary tract infections, pulmonary diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis and acne. Unless otherwise prescribed: 1-3 tablets daily taken with some liquid. In cases of known hypersensitivity to Penicillium chrysogenum, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Notakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application: Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

Do not administer simultaneously with Mucokehl. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

161

Advice:

Notakehl is used in isopathic therapy for all acute and chronic diseases caused by streptococcal or staphylococcal infections. Apply Notakehl as an interposition with herpes zoster; changing after one week to Quentakehl. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X, 30 g tube of ointment 3X.

How supplied:

162

Notakehl 4X
Capsules
For oral intake

Active ingredient: Composition:

Penicillium chrysogenum extract 4X 1 capsule contains: Medically active substance: 330 mg Penicillium chrysogenum 4X trit. Other constituents: lactose, hypromellosis (capsule shell). Notakehl is produced from the Penicillium chrysogenum mold fungus. It is not an antibiotic and does not produce antibiotic substances, therefore, there are no side effects which may occur during a treatment with antibiotics, such as allergies, liver damages, destruction of intestinal flora and the formation of Penicillin resistant strains. Notakehl specifically acts with all infections caused by streptococci and staphylococci. With alternating applications of Mucokehl or Nigersan, Notakehl plays an important role for irritative therapy. It is not only useful in cases of unsatisfactory healing processes but also with serial applications of Mucokehl during the injections intervals, to administer Notakehl or Quentakehl in any preferred dosage form. For all general bacterial suppurations, e.g. angina tonsillitis, laryngitis; follow-up treatment for suppurations caused after tooth extractions, consecutive spinal conditions e.g. cervical spine, lumbal syndrome, otitis, neuritis, neuralgia; conditions of the urogenital system e.g. adenoma of the prostate, urinary tract infections, pulmonary diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis and acne. Unless otherwise prescribed: 1-3 capsules daily taken with some liquid. In cases of known hypersensitivity to Penicillium chrysogenum, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Notakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application: Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

Do not administer simultaneously with Mucokehl. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

163

Advice:

Notakehl is used in isopathic therapy for all acute and chronic diseases caused by streptococcal or staphylococcal infections. Apply Notakehl as an interposition with herpes zoster; changing after one week to Quentakehl. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X, 30 g tube of ointment 3X.

How supplied:

164

Notakehl 3X
Suppositories

Active ingredient: Composition:

Penicillium chrysogenum extract 3X 1 suppository contains: Medically active substance: 0.2 g Penicillium chrysogenum 3X trit. Other constituents: hard fat, lactose. Notakehl is produced from the Penicillium chrysogenum mold fungus. It is not an antibiotic and does not produce antibiotic substances, therefore, there are no side effects which may occur during a treatment with antibiotics, such as allergies, liver damages, destruction of intestinal flora and the formation of Penicillin resistant strains. Notakehl specifically acts with all infections caused by streptococci and staphylococci. With alternating applications of Mucokehl or Nigersan, Notakehl plays an important role for irritative therapy. It is not only useful in cases of unsatisfactory healing processes but also with serial applications of Mucokehl during the injections intervals, to administer Notakehl or Quentakehl in any preferred dosage form. For all general bacterial suppurations, e.g. angina tonsillitis, laryngitis; follow-up treatment for suppurations caused after tooth extractions, consecutive spinal conditions e.g. cervical spine, lumbal syndrome, otitis, neuritis, neuralgia; conditions of the urogenital system e.g. adenoma of the prostate, urinary tract infections, pulmonary diseases, such as asthma-bronchitis, bronchitis, sino-bronchitis and acne. Unless otherwise prescribed: 1x daily, insert 1 suppository rectally at bedtime. In cases of known hypersensitivity to Penicillium chrysogenum, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Notakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

Do not administer simultaneously with Mucokehl. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

165

Advice:

Notakehl is used in isopathic therapy for all acute and chronic diseases caused by streptococcal or staphylococcal infections. When Notakehl 3X suppositories are administered for prostatitis, swelling of the prostate and tumors with an unspecific genesis, then alternating treatment with Mucokehl, Nigersan and Pefrakehl is useful. Apply Notakehl as an interposition with herpes zoster; changing after one week to Quentakehl. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X, 30 g tube of ointment 3X.

How supplied:

166

Notakehl 3X
Ointment

Active ingredient: Composition:

Penicillium chrysogenum extract 3X 1 g ointment contains: Medically active substance: 0.1 g Penicillium chrysogenum 3X dil. Other constituents: 0.38 g Lanolin alcohol ointment, 0.1 g Coconut oil fract., 0.03 g Glyceryl monostearate 40-50%, 0.23 g Propylene glycol, 0.02 g Magnesium sulphate x 7 H2O, 0.01 g Lactic acid, 0.13 g water for injection. Notakehl is produced from the Penicillium chrysogenum mold fungus. It is not an antibiotic and does not produce antibiotic substances, therefore, there are no side effects which may occur during a treatment with antibiotics, such as allergies, liver damages, destruction of intestinal flora and the formation of Penicillin resistant strains. Notakehl specifically acts with all infections caused by streptococci and staphylococci. With alternating applications of Mucokehl or Nigersan, Notakehl plays an important role for irritative therapy. It is not only useful in cases of unsatisfactory healing processes but also with serial applications of Mucokehl during the injections intervals, to administer Notakehl or Quentakehl in any preferred dosage form. For all general bacterial suppurations, joint afflictions, epicondylitis, consecutive spinal conditions, neuritis, ischialgia, acne, herpes zoster.

Characteristics:

According to experience, to be administered in cases of: Application: Contraindications:

Unless otherwise prescribed: Apply on the affected area 1 to 3 x daily. In cases of known hypersensitivity to Penicillium chrysogenum, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Notakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

Do not administer simultaneously with Mucokehl. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

167

Advice:

Notakehl is used in isopathic therapy for all acute and chronic diseases caused by streptococcal or staphylococcal infections. Apply Notakehl as an interposition with herpes zoster; changing after one week to Quentakehl. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 6X, 7X, 10 suppositories 3X, 20 capsules 4X, 20 tablets 5X, 30 g tube of ointment 3X.

How supplied:

168

Okoubasan 2X
Drops
Liquid dilution for oral intake

Active ingredient: Composition:

Okoubaka aubrevillei extract 2X 1 ml liquid dilution contains: Medically active substance: 1 ml Okoubaka aubrevillei 2X dil. Other constituents: purified water, ethanol. Okoubasan is produced from the dried bark of Okoubaka aubrevillei, a tree, which is mainly found in West Africa. In popular medicine, the pulverized bark is internally administered as a detoxicant. This old natives remedy was used by the Chieftans food tasters in order to protect them from poisoning. Today, Okoubaka aubrevillei is also used in the treatment of food poisoning and the healing of infectious diseases of the gastrointestinal tract. Due to its contents of tannin, catechols and phenylcarbonic acids, this plant is a typical tannin drug with strong phagocytosis promoting effects. Acute diarrhea, especially after food poisoning, infections of the gastrointestinal tract, food intolerances, prophylactic for change of nutrition and climate, during a regulation therapy for elimination of metabolic waste products. Unless otherwise prescribed: For oral intake: Adults: in case of acute conditions 5 drops every half to one hour (max. 12 times per day), for chronic forms 1-3 x daily 5 drops. None known. None known. Because of specific organic components of Okoubasan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications: Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The preparation contains 70 % (v/v) alcohol (ethanol). The following dosage forms are available: 10 ml dropper bottle 2X, 80 tablets 2X.

Duration of treatment: Advice: How supplied:

169

Okoubasan 2X
Tablets

Active ingredient: Composition:

Okoubaka aubrevillei extract 2X 1 tablet contains: Medically active substance: 250 mg Okoubaka aubrevillei 2X trit. Other constituents: lactose, potato starch, magnesium stearate. Okoubasan is produced from the dried bark of Okoubaka aubrevillei, a tree, which is mainly found in West Africa. In popular medicine, the pulverized bark is internally administered as a detoxicant. This old natives remedy was used by the Chieftans food tasters in order to protect them from poisoning. Today, Okoubaka aubrevillei is also used in the treatment of food poisoning and the healing of infectious diseases of the gastrointestinal tract. Due to its contents of tannin, catechols and phenylcarbonic acids, this plant is a typical tannin drug with strong phagocytosis promoting effects. Acute diarrhea, especially after food poisoning, infections of the gastointestinal tract, food intolerances, prophylactic for change of nutrition and climate, during a regulation therapy for elimination of metabolic waste products. Unless otherwise prescribed: For oral intake: Adults: In case of acute conditions: 1 tablet every half to one hour (max. 12 times per day), for chronic forms: 1-3 x daily 1 tablet; children should not get more than 2/3 of the dosage for adults. None known. None known. Because of specific organic components of Okoubasan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications: Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 2X, 80 tablets 2X.

Duration of treatment: How supplied:

170

Pefrakehl 5X
Drops
Liquid dilution for oral intake, rubbing in, inhalation

Active ingredient: Composition:

Candida parapsilosis extract 5X 1 ml liquid dilution contains: Medically active substance: 1 ml Candida parapsilosis 5X dil. Other constituents: purified water. Pefrakehl is produced from the yeast extract of Candida parapsilosis. According to the principle of isopathy, this preparation can restore a symbiosis (e.g. candidiasis pathogens and the mammal organism) between cohabitants of plant origin. According to Enderlein, this is a process where higher developmental forms of pathogenic yeasts are treated with lower stages of the same cyclode. Isopathic remedies can cause reactions that should not be interrupted and should normally disappear after a few days, providing some information on the type of disease and the possibility of its elimination. For all enteral mycoses, especially Candida mycoses, and their secondary diseases such as dermatomycoses, genital mycoses, all bacterial and viral diseases of the mouth, such as rhagades, aphthae, pemphigus vulgaris, dental granuloma, lymphadenitis, cystitis, etc., gastroenteritis and otitis externa, hepatopathy, after a treatment with Fortakehl over two weeks Pefrakehl is given to rebuild an enteral symbiosis. Unless otherwise prescribed: For oral intake: 1x daily 5-10 drops before a meal. For rubbing in: 1x daily 5-10 drops at the location of the disease or into the bend of the elbow. In case of simultaneous treatment with injections, rub in 2x weekly 5-10 drops on injection-free days. For inhalation: 10-20 drops, inhale deeply 2-3x daily. In cases of known hypersensitivity to Candida parapsilosis, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Pefrakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

171

Duration of treatment: Advice:

Dependent on the advice of the physician or health care professional.

Candida parapsilosis is also an active ingredient of the combination preparation Exmykehl.


The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 6X, 10 suppositories 3X, 20 capsules 4X, 30 g tube of ointment 3X.

How supplied:

172

Pefrakehl
Ampules

6X

Liquid dilution for injection

Active ingredient: Composition:

Candida parapsilosis extract 6X 1 ampule of 1 ml contains: Medically active substance: 1 ml Candida parapsilosis 6X aqueous dilut. Other constituents: isotonic sodium chloride solution. Pefrakehl is produced from the yeast extract of Candida parapsilosis. According to the principle of isopathy, this preparation can restore a symbiosis (e.g. candidiasis pathogens and the mammal organism) between cohabitants of plant origin. According to Enderlein, this is a process where higher developmental forms of pathogenic yeasts are treated with lower stages of the same cyclode. Isopathic remedies can cause reactions that should not be interrupted and should normally disappear after a few days, providing some information on the type of disease and the possibility of its elimination. For all enteral mycoses, especially Candida mycoses, and their secondary diseases such as dermatomycoses, genital mycoses, all bacterial and viral diseases of the mouth, such as rhagades, aphthae, pemphigus vulgaris, dental granuloma, lymphadenitis, cystitis, etc., gastroenteritis and otitis externa, hepatopathy, after a treatment with Fortakehl over two weeks Pefrakehl is given to rebuild an enteral symbiosis. Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intramuscularly, subcutaneously, intracutaneously or intravenously, 2x weekly. In cases of known hypersensitivity to Candida parapsilosis, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Pefrakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

173

Advice:

Candida parapsilosis is also an active ingredient of the combination preparation Exmykehl.


The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 6X, 10 suppositories 3X, 20 capsules 4X, 30 g tube of ointment 3X.

How supplied:

174

Pefrakehl 4X
Capsules
For oral intake

Active ingredient: Composition:

Candida parapsilosis extract 4X 1 capsule contains: Medically active substance: 330 mg Candida parapsilosis 4X trit. Other constituents: lactose, hypromellosis (capsule shell). Pefrakehl is produced from the yeast extract of Candida parapsilosis. According to the principle of isopathy, this preparation can restore a symbiosis (e.g. candidiasis pathogens and the mammal organism) between cohabitants of plant origin. According to Enderlein, this is a process where higher developmental forms of pathogenic yeasts are treated with lower stages of the same cyclode. Isopathic remedies can cause reactions that should not be interrupted and should normally disappear after a few days, providing some information on the type of disease and the possibility of its elimination. For all enteral mycoses, especially Candida mycoses, and their secondary diseases such as dermatomycoses, genital mycoses, all bacterial and viral diseases of the mouth, such as rhagades, aphthae, pemphigus vulgaris, dental granuloma, lymphadenitis, cystitis, etc., gastroenteritis and otitis externa, hepatopathy, after a treatment with Fortakehl over two weeks Pefrakehl is given to rebuild an enteral symbiosis. Unless otherwise prescribed: 1-3 capsules daily taken with some liquid. In cases of known hypersensitivity to Candida parapsilosis, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Pefrakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application: Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

175

Advice:

Candida parapsilosis is also an active ingredient of the combination preparation Exmykehl.


The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 6X, 10 suppositories 3X, 20 capsules 4X, 30 g tube of ointment 3X.

How supplied:

176

Pefrakehl 3X
Suppositories

Active ingredient: Composition:

Candida parapsilosis extract 3X 1 suppository contains: Medically active substance: 0. 2 g Candida parapsilosis 3X trit. Other constituents: hard fat, lactose. Pefrakehl is produced from the yeast extract of Candida parapsilosis. According to the principle of isopathy, this preparation can restore a symbiosis (e.g. candidiasis pathogens and the mammal organism) between cohabitants of plant origin. According to Enderlein, this is a process where higher developmental forms of pathogenic yeasts are treated with lower stages of the same cyclode. Isopathic remedies can cause reactions that should not be interrupted and should normally disappear after a few days, providing some information on the type of disease and the possibility of its elimination. For all enteral mycoses, especially Candida mycoses, and their secondary diseases such as dermatomycoses, genital mycoses, all bacterial and viral diseases of the mouth, such as rhagades, aphthae, pemphigus vulgaris, dental granuloma, lymphadenitis, cystitis, etc., gastroenteritis and otitis externa, hepatopathy, after a treatment with Fortakehl over two weeks Pefrakehl is given to rebuild an enteral symbiosis. Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally at bedtime. In cases of known hypersensitivity to Candida parapsilosis, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Pefrakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

177

Advice:

Candida parapsilosis is also an active ingredient of the combination preparation Exmykehl.


The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 6X, 10 suppositories 3X, 20 capsules 4X, 30 g tube of ointment 3X.

How supplied:

178

Pefrakehl 3X
Ointment

Active ingredient: Composition:

Candida parapsilosis 3X 1 g ointment contains: Medically active substance: 0.1 g Candida parapsilosis 3X dil. Other constituents: 0.38 g Lanolin alcohol ointment, 0.1 g Coconut oil fract., 0.03 g Glyceryl monostearate 40-50%, 0.23 g Propylene glycol, 0.02 g Magnesium sulphate x 7 H2O, 0.01 g Lactic acid, 0.13 g water for injection. Pefrakehl is produced from the yeast extract of Candida parapsilosis. According to the principle of isopathy, this preparation can restore a symbiosis (e.g. candidiasis pathogens and the mammal organism) between cohabitants of plant origin. According to Enderlein, this is a process where higher developmental forms of pathogenic yeasts are treated with lower stages of the same cyclode. Isopathic remedies can cause reactions that should not be interrupted and should normally disappear after a few days, providing some information on the type of disease and the possibility of its elimination. For all enteral mycoses, especially Candida mycoses, and their secondary diseases such as dermatomycoses, genital mycoses, otitis externa and acne. Unless otherwise prescribed: Apply on the affected area 1 to 3 x daily. In cases of known hypersensitivity to Candida parapsilosis, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Pefrakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application: Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

179

Advice:

Candida parapsilosis is also an active ingredient of the combination preparation Exmykehl.


The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 6X, 10 suppositories 3X, 20 capsules 4X, 30 g tube of ointment 3X.

How supplied:

180

Pinikehl 5X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Fomitopsis pinicola extract 5X 1 ml liquid dilution contains: Medically active substance: 1 ml Fomitopsis pinicola e mycelio 5X dil. Other constituents: purified water. While the sporophores of this tree-fungus have long been used in popular medicine for the production of remedies, Sanum research has succeeded in the development of a preparation which is analogous to the already proven fungal mold preparations according to Prof. Enderlein. Diseases of the liver and spleen, intermittent fever.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops before a meal. For rubbing in: 1 x daily 5-10 drops at the location of the disease or into the bend of the elbow. In case of simultaneous treatment with injections, rub in 2 x weekly 5-10 drops on injection-free days. In cases of known hypersensitivity to Fomitopsis pinicola, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Pinikehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

Duration of treatment: How supplied:

181

Pinikehl 5X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Fomitopsis pinicola extract 5X 1 ampule of 1 ml contains: Medically active substance: 1 ml Fomitopsis pinicola e mycelio 5X aqueous dilut. Other constituents: isotonic sodium chloride solution. While the sporophores of this tree-fungus have long been used in popular medicine for the production of remedies, Sanum research has succeeded in the development of a preparation which is analogous to the already proven fungal mold preparations according to Prof. Enderlein. Diseases of the liver and spleen, intermittent fever.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intramuscularly, subcutaneously, intracutaneously or intravenously, 2x weekly. In cases of known hypersensitivity to Fomitopsis pinicola, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Pinikehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

Duration of treatment: How supplied:

182

Pinikehl 4X
Capsules
For oral intake

Active ingredient: Composition:

Fomitopsis pinicola extract 4X 1 capsule contains: Medically active substance: 330 mg Fomitopsis pinicola e mycelio 4X trit. Other constituents: lactose, hypromellosis (capsule shell). While the sporophores of this tree-fungus have long been used in popular medicine for the production of remedies, Sanum research has succeeded in the development of a preparation which is analogous to the already proven fungal mold preparations according to Prof. Enderlein. Diseases of the liver and spleen, intermittent fever.

Characteristics:

According to experience, to be administered in cases of: Application: Contraindications:

Unless otherwise prescribed: 1-3 capsules daily taken with some liquid. In cases of known hypersensitivity to Fomitopsis pinicola, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Pinikehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

Duration of treatment: How supplied:

183

Pinikehl 4X
Suppositories

Active ingredient: Composition:

Fomitopsis pinicola extract 4X 1 suppository contains: Medically active substance: 0.2 g Fomitopsis pinicola e mycelio 4X trit. Other constituents: hard fat, lactose. While the sporophores of this tree-fungus have long been used in popular medicine for the production of remedies, Sanum research has succeeded in the development of a preparation which is analogous to the already proven fungal mold preparations according to Prof. Enderlein. Diseases of the liver and spleen, intermittent fever.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1x daily, insert 1 suppository rectally at bedtime. In cases of known hypersensitivity to Fomitopsis pinicola, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Pinikehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

Duration of treatment: How supplied:

184

Pleo Chelate 2X
Drops
Liquid dilution for oral intake

Active ingredient:

Sodium edetate 2X, Hydrogen peroxide 2X, Magnesium sulphate 2X, Potassium chloride 2X, Sodium chloride 2X. 100 g solution contains: Medically active substances: 8 g Sodium edetate 2X, 8 g Hydrogen peroxide 2X, 4 g Magnesium sulphate 2X, 4 g Potassium chloride 2X, 1.6 g Sodium chloride 2X. Other constituents: purified water, ethanol. Pleo Chelate is able to stimulate the bodys capacity of chelating and secreting ionic metals and particularly heavy metals such as mercury, lead and cadmium, thereby it reducing the production of harmful free radicals. Experience regarding the use of the ingredients show that essential minerals such as calcium, magnesium, potassium, sodium and selenium are not affected and copper and zinc stay within physiological limits. Reducing of high burden with heavy metals (e.g. lead in the air, mercury in tooth fillings, high levels of metals in drinking water, etc.)

Composition:

Characteristics:

According to experience, to be administered in cases of: Application:

Adults: Start with 5-30 drops daily according to individual sensitivity and increase to 3x 10 in case of low heavy metal burden, 3x 20 in case of medium heavy metal burden, 3x 30 in case of high heavy metal burden. Children (5-10 years): 5-10 drops 3x daily. The drops should be given into a glass of water with low mineral contents. Test of individual sensitivity towards PleoChelate: Rub in 5-10 drops into the bend of the elbow. In case of skin reddening after 10 minutes, start with lowest dosage and increase slowly. Do not use during pregnancy. Do not use in cases of known hypersensitivity against sodium edetate. Possible interference with chemotherapeutics, therefore, avoid drinking Pleo Chelate during chemotherapy. Slight myalgia, pruritus, xerostomia or sensation of dizziness are possible during a high Pleo Chelate administration. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. In case of increased zinc, copper, lead use up to 3 bottles. In case of increased cadmium, mercury use up to 5-6 bottles.

Contraindications: Adverse reactions: Interactions with other remedies: Side effects:

Precautions:

Duration of treatment:

185

Advice:

Drinking of sufficient fluid supports elimination of heavy metals, which are bound by Pleo Chelate. Pleo Chelate helps the body to cope better with environmental, i.e. ionic heavy metals. In case of a Pleo Chelate therapy Selenokehl, Mapurit and Zinkokehl should be applied in addition to regulate the mineral household. This preparation contains 3% (m/m) alcohol. 100 ml dropper bottle

How supplied:

186

Polysan A 9X
Drops
Liquid dilution for diagnosis, rubbing in

Active ingredient: Composition:

Spengler colloid A 9X 1 ml liquid dilution contains: Medically active substance: 1 ml Spengler colloid A 9X according to Dr. Carl Spengler with antigens of Mycobacterium tuberculosis typus bovinus, Mycobacterium tuberculosis typus brevis as well as with the respective antitoxins from the blood of highly immunized rabbits. The Polysans can be used therapeutically and also diagnostically. Carl Spengler, M.D., isolated in chronic diseases such as tuberculosis, rheumatism, cancer, etc. gram-positive and gram-negative granula from erythrocytes which he described as blood-parasites. According to Spengler, the gram-positive malignant granula disturb the binding of oxygen to hemoglobin by their fermentation thus endangering the formation of defensive substances. It was his conviction that erythrocytes that were attacked by granula are the carriers of both inherited and endogenic toxins. These specific inherited allergies are transferred from the mothers blood onto the child and may burden the descendants over several generations. After cultivating the granula in special culture-media, Dr. Spengler produced a vaccine which, in its homeopathically potentized form, was suitable as a therapeutic agent for chronic infections and for active immunization. When antibodies are present in human blood due to a former disease, they react with the respective Spengler-colloid in the sense of an antigen-antibody-reaction. This reaction is used in the diagnostic blood test (developed by Schwarz). By using the Polysans the body is stimulated to an intensified specific immune defense. It must be noted that local complaints do not necessarily indicate chronic foci. However, these must in each case be therapeutically treated, because they are permanent disturbance fields and, as such, they block the endogenic regulation of the organism. Complaints due to aging, metabolic disorders, arteriosclerosis, hypertension, cardiac affections, nervous disorders, paradontosis, prostatic diseases. Unless otherwise prescribed: For rubbing in: 3 x daily 5-10 drops into the bend of the elbow. In case of severe states begin with 5 drops 1x daily and increase the dosage. For diagnosis: A drop of the blood to be tested is mixed with a drop of the Polysan-antigens specified for the particular testing. Macroscopically and microscopically visible agglutination occurs in the case of an antigen-antibody reaction. At the same time, the degree of agglutination is an indicator of the level of antibody titer. None known.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

187

Adverse reactions:

None known. Because of specific organic components of Polysan A, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage form is available: 10 ml dropper bottle.

Duration of treatment: How supplied:

188

Polysan D 9X
Drops
Liquid dilution for diagnosis, rubbing in

Active ingredient: Composition:

Spengler colloid D 9X 1 ml liquid dilution contains: Medically active substance: 1 ml Spengler colloid D 9X according to Dr. Carl Spengler with antigens from Streptococcus lacticus, -pyogenes, -hemolyticus, -viridans, Staphylococcus albus, -pharyngis, -aureus, Diplococcus lanceolatus, Mycobacterium tuberculosis typus bovinus, increased through bacterial lysins as well as with the respective antitoxins from the blood of highly immunized rabbits. The Polysans can be used therapeutically and also diagnostically. Carl Spengler, M.D., isolated in chronic diseases such as tuberculosis, rheumatism, cancer, etc. gram-positive and gram-negative granula from erythrocytes which he described as blood-parasites. According to Spengler, the gram-positive malignant granula disturb the binding of oxygen to hemoglobin by their fermentation thus endangering the formation of defensive substances. It was his conviction that erythrocytes that were attacked by granula are the carriers of both inherited and endogenic toxins. These specific inherited allergies are transferred from the mothers blood onto the child and may burden the descendants over several generations. After cultivating the granula in special culture-media, Dr. Spengler produced a vaccine which, in its homeopathically potentized form, was suitable as a therapeutic agent for chronic infections and for active immunization. When antibodies are present in human blood due to a former disease, they react with the respective Spengler-colloid in the sense of an antigen-antibody-reaction. This reaction is used in the diagnostic blood test (developed by Schwarz). By using the Polysans the body is stimulated to an intensified specific immune defense. It must be noted that local complaints do not necessarily indicate chronic foci. However, these must in each case be therapeutically treated, because they are permanent disturbance fields and, as such, they block the endogenic regulation of the organism. Focal infections (in alternation with Polysan Dx).

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For rubbing in: 3 x daily 5-10 drops into the bend of the elbow. In case of severe states begin with 5 drops 1x daily and increase the dosage. For diagnosis: A drop of the blood to be tested is mixed with a drop of the Polysan-antigens specified for the particular testing. Macroscopically and microscopically visible agglutination occurs in the case of an antigen-antibody reaction. At the same time, the degree of agglutination is an indicator of the level of antibody titer.

189

Contraindications: Adverse reactions:

None known. None known. Because of specific organic components of Polysan D, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage form is available: 10 ml dropper bottle.

Duration of treatment: How supplied:

190

Polysan Dx 9X
Drops
Liquid dilution for diagnosis, rubbing in

Active ingredient: Composition:

Spengler colloid Dx 9X 1 ml liquid dilution contains: Medically active substance: 1 ml Spengler colloid Dx 9X according to Dr. Carl Spengler with antigens from Streptococcus lanceolatus, Staphylococcus aureus, Diplococcus pneumoniae, increased through bacterial lysins. The Polysans can be used therapeutically and also diagnostically. Carl Spengler, M.D., isolated in chronic diseases such as tuberculosis, rheumatism, cancer, etc. gram-positive and gram-negative granula from erythrocytes which he described as blood-parasites. According to Spengler, the gram-positive malignant granula disturb the binding of oxygen to hemoglobin by their fermentation thus endangering the formation of defensive substances. It was his conviction that erythrocytes that were attacked by granula are the carriers of both inherited and endogenic toxins. These specific inherited allergies are transferred from the mothers blood onto the child and may burden the descendants over several generations. After cultivating the granula in special culture-media, Dr. Spengler produced a vaccine which, in its homeopathically potentized form, was suitable as a therapeutic agent for chronic infections and for active immunization. When antibodies are present in human blood due to a former disease, they react with the respective Spengler-colloid in the sense of an antigen-antibody-reaction. This reaction is used in the diagnostic blood test (developed by Schwarz). By using the Polysans the body is stimulated to an intensified specific immune defense. It must be noted that local complaints do not necessarily indicate chronic foci. However, these must in each case be therapeutically treated, because they are permanent disturbance fields and, as such, they block the endogenic regulation of the organism. Latent focal infections (in alternation with Polysan D).

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For rubbing in: 3 x daily 5-10 drops into the bend of the elbow. In case of severe states begin with 5 drops 1x daily and increase the dosage. For diagnosis: A drop of the blood to be tested is mixed with a drop of the Polysan-antigens specified for the particular testing. Macroscopically and microscopically visible agglutination occurs in the case of an antigen-antibody reaction. At the same time, the degree of agglutination is an indicator of the level of antibody titer. None known.

Contraindications:

191

Adverse reactions:

None known. Because of specific organic components of Polysan Dx, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage form is available: 10 ml dropper bottle.

Duration of treatment: How supplied:

192

Polysan E 9X
Drops
Liquid dilution for diagnosis, rubbing in

Active ingredient: Composition:

Spengler colloid E 9X 1 ml liquid dilution contains: Medically active substance: 1 ml Spengler colloid E 9X according to Dr. Carl Spengler with antigens from luetic hereditary toxins. The Polysans can be used therapeutically and also diagnostically. Carl Spengler, M.D., isolated in chronic diseases such as tuberculosis, rheumatism, cancer, etc. gram-positive and gram-negative granula from erythrocytes which he described as blood-parasites. According to Spengler, the gram-positive malignant granula disturb the binding of oxygen to hemoglobin by their fermentation thus endangering the formation of defensive substances. It was his conviction that erythrocytes that were attacked by granula are the carriers of both inherited and endogenic toxins. These specific inherited allergies are transferred from the mothers blood onto the child and may burden the descendants over several generations. After cultivating the granula in special culture-media, Dr. Spengler produced a vaccine which, in its homeopathically potentized form, was suitable as a therapeutic agent for chronic infections and for active immunization. When antibodies are present in human blood due to a former disease, they react with the respective Spengler-colloid in the sense of an antigen-antibody-reaction. This reaction is used in the diagnostic blood test (developed by Schwarz). By using the Polysans the body is stimulated to an intensified specific immune defense. It must be noted that local complaints do not necessarily indicate chronic foci. However, these must in each case be therapeutically treated, because they are permanent disturbance fields and, as such, they block the endogenic regulation of the organism. Inherited toxins, especially of luetic nature.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For rubbing in: 3 x daily 5-10 drops into the bend of the elbow. In case of severe states begin with 5 drops 1x daily and increase the dosage. For diagnosis: A drop of the blood to be tested is mixed with a drop of the Polysan-antigens specified for the particular testing. Macroscopically and microscopically visible agglutination occurs in the case of an antigen-antibody reaction. At the same time, the degree of agglutination is an indicator of the level of antibody titer. None known.

Contraindications:

193

Adverse reactions:

None known. Because of specific organic components of Polysan E, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage form is available: 10 ml dropper bottle.

Duration of treatment: How supplied:

194

Polysan G 9X
Drops
Liquid dilution for diagnosis, rubbing in

Active ingredient: Composition:

Spengler colloid G 9X 1 ml liquid dilution contains: Medically active substance: 1 ml Spengler colloid G 9X according to Dr. Carl Spengler with antigens from Virus influenzae Spengler, Bazillus influenzae Pfeiffer, Bacterium pneumoniae as well as with the respective antitoxins from the blood of highly immunized rabbits. The Polysans can be used therapeutically and also diagnostically. Carl Spengler, M.D., isolated in chronic diseases such as tuberculosis, rheumatism, cancer, etc. gram-positive and gram-negative granula from erythrocytes which he described as blood-parasites. According to Spengler, the gram-positive malignant granula disturb the binding of oxygen to hemoglobin by their fermentation thus endangering the formation of defensive substances. It was his conviction that erythrocytes that were attacked by granula are the carriers of both inherited and endogenic toxins. These specific inherited allergies are transferred from the mothers blood onto the child and may burden the descendants over several generations. After cultivating the granula in special culture-media, Dr. Spengler produced a vaccine which, in its homeopathically potentized form, was suitable as a therapeutic agent for chronic infections and for active immunization. When antibodies are present in human blood due to a former disease, they react with the respective Spengler-colloid in the sense of an antigen-antibody-reaction. This reaction is used in the diagnostic blood test (developed by Schwarz). By using the Polysans the body is stimulated to an intensified specific immune defense. It must be noted that local complaints do not necessarily indicate chronic foci. However, these must in each case be therapeutically treated, because they are permanent disturbance fields and, as such, they block the endogenic regulation of the organism. Flu, angina, suppurations, all inflammations, blood poisoning, feverish diseases, diverse colds.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For rubbing in: 3 x daily 5-10 drops into the bend of the elbow. In case of severe states begin with 5 drops 1x daily and increase the dosage. For diagnosis: A drop of the blood to be tested is mixed with a drop of the Polysan-antigens specified for the particular testing. Macroscopically and microscopically visible agglutination occurs in the case of an antigen-antibody reaction. At the same time, the degree of agglutination is an indicator of the level of antibody titer. None known.

Contraindications:

195

Adverse reactions:

None known. Because of specific organic components of Polysan G, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage form is available: 10 ml dropper bottle.

Duration of treatment: How supplied:

196

Polysan K 9X
Drops
Liquid dilution for diagnosis, rubbing in

Active ingredient: Composition:

Spengler colloid K 9X 1 ml liquid dilution contains: Medically active substance: 1 ml Spengler colloid K 9X according to Dr. Carl Spengler with antigens from Streptococcus lanceolatus, Staphylococcus aureus, Diplococcus pneumoniae as well as with the respective antitoxins from the blood of highly immunized rabbits. The Polysans can be used therapeutically and also diagnostically. Carl Spengler, M.D., isolated in chronic diseases such as tuberculosis, rheumatism, cancer, etc. gram-positive and gram-negative granula from erythrocytes which he described as blood-parasites. According to Spengler, the gram-positive malignant granula disturb the binding of oxygen to hemoglobin by their fermentation thus endangering the formation of defensive substances. It was his conviction that erythrocytes that were attacked by granula are the carriers of both inherited and endogenic toxins. These specific inherited allergies are transferred from the mothers blood onto the child and may burden the descendants over several generations. After cultivating the granula in special culture-media, Dr. Spengler produced a vaccine which, in its homeopathically potentized form, was suitable as a therapeutic agent for chronic infections and for active immunization. When antibodies are present in human blood due to a former disease, they react with the respective Spengler-colloid in the sense of an antigen-antibody-reaction. This reaction is used in the diagnostic blood test (developed by Schwarz). By using the Polysans the body is stimulated to an intensified specific immune defense. It must be noted that local complaints do not necessarily indicate chronic foci. However, these must in each case be therapeutically treated, because they are permanent disturbance fields and, as such, they block the endogenic regulation of the organism. Circulatory disorders, venous congestion, allergic illnesses (asthma, hay fever), varicose veins, pre-cancerous stages.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For rubbing in: 3 x daily 5-10 drops into the bend of the elbow. In case of severe states begin with 5 drops 1x daily and increase the dosage. For diagnosis: A drop of the blood to be tested is mixed with a drop of the Polysan-antigens specified for the particular testing. Macroscopically and microscopically visible agglutination occurs in the case of an antigen-antibody reaction. At the same time, the degree of agglutination is an indicator of the level of antibody titer. None known.

Contraindications:

197

Adverse reactions:

None known. Because of specific organic components of Polysan K, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage form is available: 10 ml dropper bottle.

Duration of treatment: How supplied:

198

Polysan M 9X
Drops
Liquid dilution for diagnosis, rubbing in

Active ingredient: Composition:

Spengler colloid M 9X 1 ml liquid dilution contains: Medically active substance: 1 ml Spengler colloid M 9X according to Dr. Carl Spengler with antigens from malaria plasmodia as well as with the respective antitoxins from the blood of highly immunized rabbits. The Polysans can be used therapeutically and also diagnostically. Carl Spengler, M.D., isolated in chronic diseases such as tuberculosis, rheumatism, cancer, etc. gram-positive and gram-negative granula from erythrocytes which he described as blood-parasites. According to Spengler, the gram-positive malignant granula disturb the binding of oxygen to hemoglobin by their fermentation thus endangering the formation of defensive substances. It was his conviction that erythrocytes that were attacked by granula are the carriers of both inherited and endogenic toxins. These specific inherited allergies are transferred from the mothers blood onto the child and may burden the descendants over several generations. After cultivating the granula in special culture-media, Dr. Spengler produced a vaccine which, in its homeopathically potentized form, was suitable as a therapeutic agent for chronic infections and for active immunization. When antibodies are present in human blood due to a former disease, they react with the respective Spengler-colloid in the sense of an antigen-antibody-reaction. This reaction is used in the diagnostic blood test (developed by Schwarz). By using the Polysans the body is stimulated to an intensified specific immune defense. It must be noted that local complaints do not necessarily indicate chronic foci. However, these must in each case be therapeutically treated, because they are permanent disturbance fields and, as such, they block the endogenic regulation of the organism. Malaria and its late effects.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For rubbing in: 3 x daily 5-10 drops into the bend of the elbow. In case of severe states begin with 5 drops 1x daily and increase the dosage. For diagnosis: A drop of the blood to be tested is mixed with a drop of the Polysan-antigens specified for the particular testing. Macroscopically and microscopically visible agglutination occurs in the case of an antigen-antibody reaction. At the same time, the degree of agglutination is an indicator of the level of antibody titer. None known.

Contraindications:

199

Adverse reactions:

None known. Because of specific organic components of Polysan M, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage form is available: 10 ml dropper bottle.

Duration of treatment: How supplied:

200

Polysan Om 9X
Drops
Liquid dilution for diagnosis, rubbing in

Active ingredient: Composition:

Spengler colloid Om 9X 1 ml liquid dilution contains: Medically active substance: 1 ml Spengler colloid Om 9X according to Dr. Carl Spengler with antigens from Streptococcus lacticus, -pyogenes, -hemolyticus, -viridans, Staphylococcus albus, -pharyngis, -aureus, Diplococcus lanceolatus, Mycobacterium tuberculosis typus bovinus as well as with the respective antitoxins from the blood of highly immunized rabbits. The Polysans can be used therapeutically and also diagnostically. Carl Spengler, M.D., isolated in chronic diseases such as tuberculosis, rheumatism, cancer, etc. gram-positive and gram-negative granula from erythrocytes which he described as blood-parasites. According to Spengler, the gram-positive malignant granula disturb the binding of oxygen to hemoglobin by their fermentation thus endangering the formation of defensive substances. It was his conviction that erythrocytes that were attacked by granula are the carriers of both inherited and endogenic toxins. These specific inherited allergies are transferred from the mothers blood onto the child and may burden the descendants over several generations. After cultivating the granula in special culture-media, Dr. Spengler produced a vaccine which, in its homeopathically potentized form, was suitable as a therapeutic agent for chronic infections and for active immunization. When antibodies are present in human blood due to a former disease, they react with the respective Spengler-colloid in the sense of an antigen-antibody-reaction. This reaction is used in the diagnostic blood test (developed by Schwarz). By using the Polysans the body is stimulated to an intensified specific immune defense. It must be noted that local complaints do not necessarily indicate chronic foci. However, these must in each case be therapeutically treated, because they are permanent disturbance fields and, as such, they block the endogenic regulation of the organism. Neoplasms, both benign and malignant, precancerous.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For rubbing in: 3 x daily 5-10 drops into the bend of the elbow. In case of severe states begin with 5 drops 1x daily and increase the dosage. For diagnosis: A drop of the blood to be tested is mixed with a drop of the Polysan-antigens specified for the particular testing. Macroscopically and microscopically visible agglutination occurs in the case of an antigen-antibody reaction. At the same time, the degree of agglutination is an indicator of the level of antibody titer.

201

Contraindications: Adverse reactions:

None known. None known. Because of specific organic components of Polysan Om, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage form is available: 10 ml dropper bottle.

Duration of treatment: How supplied:

202

Polysan R 9X
Drops
Liquid dilution for diagnosis, rubbing in

Active ingredient: Composition:

Spengler colloid R 9X 1 ml liquid dilution contains: Medically active substance: 1 ml Spengler colloid R 9X according to Dr. Carl Spengler with antigens from Mycobacterium tuberculosis typus humanus, Mycobacterium tuberculosis typus brevis, Mycobacterium tuberculosis typus bovinus, Streptococcus pyogenes as well as with the respective antitoxins from the blood of highly immunized rabbits. The Polysans can be used therapeutically and also diagnostically. Carl Spengler, M.D., isolated in chronic diseases such as tuberculosis, rheumatism, cancer, etc. gram-positive and gram-negative granula from erythrocytes which he described as blood-parasites. According to Spengler, the gram-positive malignant granula disturb the binding of oxygen to hemoglobin by their fermentation thus endangering the formation of defensive substances. It was his conviction that erythrocytes that were attacked by granula are the carriers of both inherited and endogenic toxins. These specific inherited allergies are transferred from the mothers blood onto the child and may burden the descendants over several generations. After cultivating the granula in special culture-media, Dr. Spengler produced a vaccine which, in its homeopathically potentized form, was suitable as a therapeutic agent for chronic infections and for active immunization. When antibodies are present in human blood due to a former disease, they react with the respective Spengler-colloid in the sense of an antigen-antibody-reaction. This reaction is used in the diagnostic blood test (developed by Schwarz). By using the Polysans the body is stimulated to an intensified specific immune defense. It must be noted that local complaints do not necessarily indicate chronic foci. However, these must in each case be therapeutically treated, because they are permanent disturbance fields and, as such, they block the endogenic regulation of the organism. Rheumatism, gout, neuralgia, elimination of uric acid, rheumatism of tuberculous origin.

Characteristics:

According to experience, to be administered in cases of: Indications: Application:

Unless otherwise prescribed: For rubbing in: 3 x daily 5-10 drops into the bend of the elbow. In case of severe states begin with 5 drops 1x daily and increase the dosage. For diagnosis: A drop of the blood to be tested is mixed with a drop of the Polysan-antigens specified for the particular testing. Macroscopically and microscopically visible agglutination occurs in the case of an antigen-antibody reaction. At the same time, the degree of agglutination is an indicator of the level of antibody titer.

203

Contraindications: Adverse reactions:

None known. None known. Because of specific organic components of Polysan R, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage form is available: 10 ml dropper bottle.

Duration of treatment: How supplied:

204

Polysan T 9X
Drops
Liquid dilution for diagnosis, rubbing in

Active ingredient: Composition:

Spengler colloid T 9X 1 ml liquid dilution contains: Medically active substance: 1 ml Spengler colloid T 9X according to Dr. Carl Spengler with antigens from Mycobacterium tuberculosis typus humanus, Mycobacterium tuberculosis typus brevis, Mycobacterium tuberculosis typus bovinus, Diplococcus peumoniae, Streptococcus mucosus as well as with the respective antitoxins from the blood of highly immunized rabbits. The Polysans can be used therapeutically and also diagnostically. Carl Spengler, M.D., isolated in chronic diseases such as tuberculosis, rheumatism, cancer, etc. gram-positive and gram-negative granula from erythrocytes which he described as blood-parasites. According to Spengler, the gram-positive malignant granula disturb the binding of oxygen to hemoglobin by their fermentation thus endangering the formation of defensive substances. It was his conviction that erythrocytes that were attacked by granula are the carriers of both inherited and endogenic toxins. These specific inherited allergies are transferred from the mothers blood onto the child and may burden the descendants over several generations. After cultivating the granula in special culture-media, Dr. Spengler produced a vaccine which, in its homeopathically potentized form, was suitable as a therapeutic agent for chronic infections and for active immunization. When antibodies are present in human blood due to a former disease, they react with the respective Spengler-colloid in the sense of an antigen-antibody-reaction. This reaction is used in the diagnostic blood test (developed by Schwarz). By using the Polysans the body is stimulated to an intensified specific immune defense. It must be noted that local complaints do not necessarily indicate chronic foci. However, these must in each case be therapeutically treated, because they are permanent disturbance fields and, as such, they block the endogenic regulation of the organism. Tuberculosis, its latent and masked forms as asthma, eczema, rheumatism, migraine, scrofulosis.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For rubbing in: 3 x daily 5-10 drops into the bend of the elbow. In case of severe states begin with 5 drops 1x daily and increase the dosage. For diagnosis: A drop of the blood to be tested is mixed with a drop of the Polysan-antigens specified for the particular testing. Macroscopically and microscopically visible agglutination occurs in the case of an antigen-antibody reaction. At the same time, the degree of agglutination is an indicator of the level of antibody titer.

205

Contraindications: Adverse reactions:

None known. None known. Because of specific organic components of Polysan T, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage form is available: 10 ml dropper bottle.

Duration of treatment: How supplied:

206

Quentakehl
Drops

5X

Liquid dilution for oral intake, rubbing in, inhalation

Active ingredient: Composition:

Penicillium glabrum extract 5X 1 ml liquid dilution contains: Medically active substance: 1 ml Penicillium glabrum 5X dil. Other constituents: purified water. Quentakehl is produced from the Penicillium glabrum mold fungus. It is not an antibiotic and does not produce antibiotic substances, therefore, there are no side effects which may occur during a treatment with antibiotics, such as allergies, liver damage, destruction of intestinal flora and the formation of Penicillin resistant strains. Quentakehl specifically acts with all virus infections. In simultaneous application with Mucokehl or Nigersan, Quentakehl plays an important role for irritative therapy. In serial applications with Mucokehl, it is useful to apply Quentakehl or Notakehl in any preferred administration form, not only in cases of unsatisfactory therapy healing processes, but also during injection intervals. Acute and latent viral infections, e.g. laryngitis, bronchitis, sinusitis, pharyngitis, influenza type infections, all diseases caused by mixed infections, or as an intensifier of other fungal preparations for: migraine, multiple sclerosis, vertigo, Menires disease, Herpes zoster, chicken pox, headaches and cervical spine and as an interposition with chronic inflammations of the urinary tract and nephritis when treated with fungal preparations. Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops before a meal. For rubbing in: 1 x daily 5-10 drops at the location of the disease or into the bend of the elbow. In case of simultaneous treatment with injections, rub in 2 x weekly 5-10 drops on injection-free days. For inhalation: 10-20 drops, inhaled deeply 2-3 x daily. In cases of known hypersensitivity to Penicillium glabrum, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Quentakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

207

Duration of treatment: How supplied:

Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

208

Quentakehl
Ampules
Liquid dilution for injection

5X

Active ingredient: Composition:

Penicillium glabrum extract 5X 1 ampule of 1 ml contains: Medically active substance: 1 ml Penicillium glabrum 5X aqueous dilut. Other constituents: isotonic sodium chloride solution. Quentakehl is produced from the Penicillium glabrum mold fungus. It is not an antibiotic and does not produce antibiotic substances, therefore, there are no side effects which may occur during a treatment with antibiotics, such as allergies, liver damage, destruction of intestinal flora and the formation of Penicillin resistant strains. Quentakehl specifically acts with all virus infections. In simultaneous application with Mucokehl or Nigersan, Quentakehl plays an important role for irritative therapy. In serial applications with Mucokehl, it is useful to apply Quentakehl or Notakehl in any preferred administration form, not only in cases of unsatisfactory therapy healing processes, but also during injection intervals. Acute and latent viral infections, e.g. laryngitis, bronchitis, sinusitis, pharyngitis, influenza type infections, all diseases caused by mixed infections, or as an intensifier of other fungal preparations for: migraine, multiple sclerosis, vertigo, Menires disease, Herpes zoster, chicken pox, headaches and cervical spine and as an interposition with chronic inflammations of the urinary tract and nephritis when treated with fungal preparations. Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intramuscularly, subcutaneously, intracutaneously or intravenously, 2 x weekly. In cases of known hypersensitivity to Penicillium glabrum, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Quentakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

209

Duration of treatment: How supplied:

Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

210

Quentakehl
Capsules
For oral intake

4X

Active ingredient: Composition:

Penicillium glabrum extract 4X 1 capsule contains: Medically active substance: 330 mg Penicillium glabrum 4X trit. Other constituents: lactose, hypromellosis (capsule shell). Quentakehl is produced from the Penicillium glabrum mold fungus. It is not an antibiotic and does not produce antibiotic substances, therefore, there are no side effects which may occur during a treatment with antibiotics, such as allergies, liver damage, destruction of intestinal flora and the formation of Penicillin resistant strains. Quentakehl specifically acts with all virus infections. In simultaneous application with Mucokehl or Nigersan, Quentakehl plays an important role for irritative therapy. In serial applications with Mucokehl, it is useful to apply Quentakehl or Notakehl in any preferred administration form, not only in cases of unsatisfactory therapy healing processes, but also during injection intervals. Acute and latent viral infections, e.g. laryngitis, bronchitis, sinusitis, pharyngitis, influenza type infections, all diseases caused by mixed infections, or as an intensifier of other fungal preparations for: migraine, multiple sclerosis, vertigo, Menires disease, Herpes zoster, chicken pox, headaches and cervical spine and as an interposition with chronic inflammations of the urinary tract and nephritis when treated with fungal preparations. Unless otherwise prescribed: 1-3 capsules daily taken with some liquid. In cases of known hypersensitivity to Penicillium glabrum, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Quentakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application: Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

211

Duration of treatment: How supplied:

Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

212

Quentakehl
Suppositories

3X

Active ingredient: Composition:

Penicillium glabrum extract 3X 1 suppository contains: Medically active substance: 0.2 g Penicillium glabrum 3X trit. Other constituents: hard fat, lactose. Quentakehl is produced from the Penicillium glabrum mold fungus. It is not an antibiotic and does not produce antibiotic substances, therefore, there are no side effects which may occur during a treatment with antibiotics, such as allergies, liver damage, destruction of intestinal flora and the formation of Penicillin resistant strains. Quentakehl specifically acts with all virus infections. In simultaneous application with Mucokehl or Nigersan, Quentakehl plays an important role for irritative therapy. In serial applications with Mucokehl, it is useful to apply Quentakehl or Notakehl in any preferred administration form, not only in cases of unsatisfactory therapy healing processes, but also during injection intervals. Acute and latent viral infections, e.g. laryngitis, bronchitis, sinusitis, pharyngitis, influenza type infections, all diseases caused by mixed infections, or as an intensifier of other fungal preparations for: migraine, multiple sclerosis, vertigo, Menires disease, Herpes zoster, chicken pox, headaches and cervical spine and as an interposition with chronic inflammations of the urinary tract and nephritis when treated with fungal preparations. Unless otherwise prescribed: 1x daily, insert 1 suppository rectally at bedtime. In cases of known hypersensitivity to Penicillium glabrum, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Quentakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

213

Duration of treatment: How supplied:

Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X, 20 capsules 4X.

214

Rebas 4X
Ampules
Liquid dilution for oral intake

Active ingredient: Composition:

Peyers patches extract (porcine) 4X 1 ampule of 2 ml contains: Medically active substance: 2 ml Peyers patches extract (porcine) 4X aqueous dilut. Other constituents: isotonic sodium chloride solution. The anatomist J.C. Peyer (1653-1712) of Basel, described for the first time collections of lymphatic tissue in the small intestine; later on they were named Peyers Patches. These belong to the portion of the immune system which, located within the intestinal wall, houses 70-80% of the defensive cells of the entire immune system. Due to its structure and form, including a large surface, the intestine is exposed to an enormous number of antigens. They are mainly orally absorbed substances, such as food particles and decomposition products, parasitary and viral substances, toxins and enzymes. Peyers Patches act as an immunologic place of contact for the particles which have penetrated into the interior milieu due to insufficient protection through the intestinal mucous membrane or by absorption. These antigens may cause local and systemic reactions. They are mostly taken up in the subepithelial macrophages in Peyers Patches and subsequently excreted through the mesenteric lymph nodes. Occasionally, the immunologic defensive mechanisms fail or cause damages through overreaction. The disturbed defense system facilitates infections, defective regulation, and auto- and hyper-immune reactions. Rebas is based on Peyers Patches isolated from porcine under controlled conditions and veterinary supervision. It is a remedy for the strengthening of the humoral defense and the recreation of a well functioning immune system. Immunological tests have proven its excellent stimulation of T-lymphocytes, and this activity of Rebas is comparable to the activity of isolated thymus-fractions. Chronic and recurrent inflammations which include disorders of the humoral body defense, in gastrointestinal diseases, chronic hepatitis, tonsillitis.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 2 ml to be injected either intramuscularly, subcutaneously or intracutaneously, 2 x weekly. In cases of known hypersensitivity to animal protein, especially pig protein, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Rebas, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

215

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. In some countries this preparation is only available in potency 5X. The following dosage forms are available: 2 ml ampule 10 and 50 4X (5X), 12X, 10 suppositories 4X, 6X, 20 capsules 4X, 6X.

Duration of treatment: Advice: How supplied:

216

Rebas 12X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Peyers patches extract (porcine) 12X 1 ampule of 2 ml contains: Medically active substance: 2 ml Peyers patches extract (porcine) 12X aqueous dilut. Other constituents: isotonic sodium chloride solution. The anatomist J.C. Peyer (1653-1712) of Basel, described for the first time collections of lymphatic tissue in the small intestine; later on they were named Peyers Patches. These belong to the portion of the immune system which, located within the intestinal wall, houses 70-80% of the defensive cells of the entire immune system. Due to its structure and form, including a large surface, the intestine is exposed to an enormous number of antigens. They are mainly orally absorbed substances, such as food particles and decomposition products, parasitary and viral substances, toxins and enzymes. Peyers Patches act as an immunologic place of contact for the particles which have penetrated into the interior milieu due to insufficient protection through the intestinal mucous membrane or by absorption. These antigens may cause local and systemic reactions. They are mostly taken up in the subepithelial macrophages in Peyers Patches and subsequently excreted through the mesenteric lymph nodes. Occasionally, the immunologic defensive mechanisms fail or cause damages through overreaction. The disturbed defense system facilitates infections, defective regulation, and auto- and hyper-immune reactions. Rebas is based on Peyers Patches isolated from porcine under controlled conditions and veterinary supervision. It is a remedy for the strengthening of the humoral defense and the recreation of a well functioning immune system. Immunological tests have proven its excellent stimulation of T-lymphocytes, and this activity of Rebas is comparable to the activity of isolated thymus-fractions. Chronic and recurrent inflammations which include disorders of the humoral body defense, in gastrointestinal diseases, chronic hepatitis, tonsillitis.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 2 ml to be injected either intramuscularly, subcutaneously or intracutaneously, 2 x weekly. In cases of known hypersensitivity to animal protein, especially pig protein, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Rebas, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

217

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 2 ml ampule 10 and 50 4X, 12X, 10 suppositories 4X, 6X, 20 capsules 4X, 6X.

Duration of treatment: How supplied:

218

Rebas 4X
Capsules
For oral intake

Active ingredient: Composition:

Peyers patches extract (porcine) 4X 1 capsule contains: Medically active substance: 330 mg Peyers patches extract (porcine) 4X trit. Other constituents: lactose, hypromellosis (capsule shell). The anatomist J.C. Peyer (1653-1712) of Basel, described for the first time collections of lymphatic tissue in the small intestine; later on they were named Peyers Patches. These belong to the portion of the immune system which, located within the intestinal wall, houses 70-80% of the defensive cells of the entire immune system. Due to its structure and form, including a large surface, the intestine is exposed to an enormous number of antigens. They are mainly orally absorbed substances, such as food particles and decomposition products, parasitary and viral substances, toxins and enzymes. Peyers Patches act as an immunologic place of contact for the particles which have penetrated into the interior milieu due to insufficient protection through the intestinal mucous membrane or by absorption. These antigens may cause local and systemic reactions. They are mostly taken up in the subepithelial macrophages in Peyers Patches and subsequently excreted through the mesenteric lymph nodes. Occasionally, the immunologic defensive mechanisms fail or cause damages through overreaction. The disturbed defense system facilitates infections, defective regulation, and auto- and hyper-immune reactions. Rebas is based on Peyers Patches isolated from porcine under controlled conditions and veterinary supervision. It is a remedy for the strengthening of the humoral defense and the recreation of a well functioning immune system. Immunological tests have proven its excellent stimulation of T-lymphocytes, and this activity of Rebas is comparable to the activity of isolated thymus-fractions. Chronic and recurrent inflammations which include disorders of the humoral body defense, in gastrointestinal diseases, chronic hepatitis, tonsillitis.

Characteristics:

According to experience, to be administered in cases of: Application: Contraindications: Adverse reactions:

Unless otherwise prescribed: 1-3 capsules daily before a meal. None known. None known. Because of specific organic components of Rebas, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Interactions with other remedies:

None known.

219

Side effects: Precautions:

None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 2 ml ampule 10 and 50 4X, 12X, 10 suppositories 4X, 6X, 20 capsules 4X, 6X.

Duration of treatment: How supplied:

220

Rebas 6X
Capsules
For oral intake

Active ingredient: Composition:

Peyers patches extract (porcine) 6X 1 capsule contains: Medically active substance: 330 mg Peyers patches extract (porcine) 6X trit. Other constituents: lactose, hypromellosis (capsule shell). The anatomist J.C. Peyer (1653-1712) of Basel, described for the first time collections of lymphatic tissue in the small intestine; later on they were named Peyers Patches. These belong to the portion of the immune system which, located within the intestinal wall, houses 70-80% of the defensive cells of the entire immune system. Due to its structure and form, including a large surface, the intestine is exposed to an enormous number of antigens. They are mainly orally absorbed substances, such as food particles and decomposition products, parasitary and viral substances, toxins and enzymes. Peyers Patches act as an immunologic place of contact for the particles which have penetrated into the interior milieu due to insufficient protection through the intestinal mucous membrane or by absorption. These antigens may cause local and systemic reactions. They are mostly taken up in the subepithelial macrophages in Peyers Patches and subsequently excreted through the mesenteric lymph nodes. Occasionally, the immunologic defensive mechanisms fail or cause damages through overreaction. The disturbed defense system facilitates infections, defective regulation, and auto- and hyper-immune reactions. Rebas is based on Peyers Patches isolated from porcine under controlled conditions and veterinary supervision. It is a remedy for the strengthening of the humoral defense and the recreation of a well functioning immune system. Immunological tests have proven its excellent stimulation of T-lymphocytes, and this activity of Rebas is comparable to the activity of isolated thymus-fractions. Chronic and recurrent inflammations which include disorders of the humoral body defense, in gastrointestinal diseases, chronic hepatitis, tonsillitis.

Characteristics:

According to experience, to be administered in cases of: Application: Contraindications: Adverse reactions:

Unless otherwise prescribed: 1-3 capsules daily before a meal. None known. None known. Because of specific organic components of Rebas, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Interactions with other remedies:

None known.

221

Side effects: Precautions:

None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 2 ml ampule 10 and 50 4X, 12X, 10 suppositories 4X, 6X, 20 capsules 4X, 6X

Duration of treatment: How supplied:

222

Rebas 4X
Suppositories

Active ingredient: Composition:

Peyers patches extract (porcine) 4X 1 suppository contains: Medically active substance: 0.2 g Peyers patches extract (porcine) 4X trit. Other constituents: hard fat, lactose. The anatomist J.C. Peyer (1653-1712) of Basel, described for the first time collections of lymphatic tissue in the small intestine; later on they were named Peyers Patches. These belong to the portion of the immune system which, located within the intestinal wall, houses 70-80% of the defensive cells of the entire immune system. Due to its structure and form, including a large surface, the intestine is exposed to an enormous number of antigens. They are mainly orally absorbed substances, such as food particles and decomposition products, parasitary and viral substances, toxins and enzymes. Peyers Patches act as an immunologic place of contact for the particles which have penetrated into the interior milieu due to insufficient protection through the intestinal mucous membrane or by absorption. These antigens may cause local and systemic reactions. They are mostly taken up in the subepithelial macrophages in Peyers Patches and subsequently excreted through the mesenteric lymph nodes. Occasionally, the immunologic defensive mechanisms fail or cause damages through overreaction. The disturbed defense system facilitates infections, defective regulation, and auto- and hyper-immune reactions. Rebas is based on Peyers Patches isolated from porcine under controlled conditions and veterinary supervision. It is a remedy for the strengthening of the humoral defense and the recreation of a well functioning immune system. Immunological tests have proven its excellent stimulation of T-lymphocytes, and this activity of Rebas is comparable to the activity of isolated thymus-fractions. Chronic and recurrent inflammations which include disorders of the humoral body defense, in gastrointestinal diseases, chronic hepatitis, tonsillitis.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 x daily 1 suppository to be inserted rectally at bedtime. None known. None known. Because of specific organic components of Rebas, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications: Adverse reactions:

Interactions with other remedies:

None known.

223

Side effects: Precautions:

None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 2 ml ampule 10 and 50 4X, 12X, 10 suppositories 4X, 6X, 20 capsules 4X, 6X.

Duration of treatment: How supplied:

224

Rebas 6X
Suppositories

Active ingredient: Composition:

Peyers patches extract (porcine) 6X 1 suppository contains: Medically active substance: 0.2 g Peyers patches extract (porcine) 6X trit. Other constituents: hard fat, lactose. The anatomist J.C. Peyer (1653-1712) of Basel, described for the first time collections of lymphatic tissue in the small intestine; later on they were named Peyers Patches. These belong to the portion of the immune system which, located within the intestinal wall, houses 70-80% of the defensive cells of the entire immune system. Due to its structure and form, including a large surface, the intestine is exposed to an enormous number of antigens. They are mainly orally absorbed substances, such as food particles and decomposition products, parasitary and viral substances, toxins and enzymes. Peyers Patches act as an immunologic place of contact for the particles which have penetrated into the interior milieu due to insufficient protection through the intestinal mucous membrane or by absorption. These antigens may cause local and systemic reactions. They are mostly taken up in the subepithelial macrophages in Peyers Patches and subsequently excreted through the mesenteric lymph nodes. Occasionally, the immunologic defensive mechanisms fail or cause damages through overreaction. The disturbed defense system facilitates infections, defective regulation, and auto- and hyper-immune reactions. Rebas is based on Peyers Patches isolated from porcine under controlled conditions and veterinary supervision. It is a remedy for the strengthening of the humoral defense and the recreation of a well functioning immune system. Immunological tests have proven its excellent stimulation of T-lymphocytes, and this activity of Rebas is comparable to the activity of isolated thymus-fractions. Chronic and recurrent inflammations which include disorders of the humoral body defense, in gastrointestinal diseases, chronic hepatitis, tonsillitis.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 x daily 1 suppository to be inserted rectally at bedtime. None known. None known. Because of specific organic components of Rebas, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications: Adverse reactions:

Interactions with other remedies:

None known.

225

Side effects: Precautions:

None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 2 ml ampule 10 and 50 4X, 12X, 10 suppositories 4X, 6X, 20 capsules 4X, 6X.

Duration of treatment: How supplied:

226

Recarcin 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Bacillus firmus extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Bacillus firmus 6X dil. Other constituents: purified water. Recarcin is a preparation from the Bacillus firmus, a particular strain from the group of non-pathogenic bacilli. Experience has shown that Recarcin raises the defensive capacity of a normal bacterial flora. Its content of polysaccharides, ferments, and specific protein combinations exerts a special effect of Recarcin that is to be understood in the sense of an immune- and irritative therapy. The progressing disease process is thereby blocked and the specific defense capacity is activated. In immunological test models, a significant rise in phagocytic activity has been established. A strong rise in the T-lymphocyte proliferation also confirms Recarcin as a potent immune modulator. All sub-acute and chronic inflammatory diseases, especially of the glands and serosae, arthritis and arthrosis, for immune modulation.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For oral intake: 1-3 x daily 2-8 drops before a meal. For rubbing in: 2-3 x weekly 5-10 drops at the location of the disease or into the bend of the elbow. In cases of known hypersensitivity to Bacillus firmus, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Recarcin, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. None known. An interval of 2 weeks should be kept to the administration of vaccinations. In cases of simultaneous treatment with immunosuppressive remedies, the effectiveness of Recarcin may be influenced. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

Duration of treatment:

227

Advice:

In isopathic therapy Recarcin is employed as an unspecific irritative agent for all chronic diseases. The alternating administration of Recarcin and Utilin proved a success. Also under a noticeable stimulus threshold a good effect of Recarcin is achieved. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

How supplied:

228

Recarcin 4X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Bacillus firmus extract 4X 1 ampule of 1 ml contains: Medically active substance: 1 ml Bacillus firmus 4X aqueous dilut. Other constituents: isotonic sodium chloride solution. Recarcin is a preparation from the Bacillus firmus, a particular strain from the group of non-pathogenic bacilli. Experience has shown that Recarcin raises the defensive capacity of a normal bacterial flora. Its content of polysaccharides, ferments, and specific protein combinations exerts a special effect of Recarcin that is to be understood in the sense of an immune- and irritative therapy. The progressing disease process is thereby blocked and the specific defense capacity is activated. In immunological test models, a significant rise in phagocytic activity has been established. A strong rise in the T-lymphocyte proliferation also confirms Recarcin as a potent immune modulator. All sub-acute and chronic inflammatory diseases, especially of the glands and serosae, arthritis and arthrosis, for immune modulation.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 1 ml to be injected deeply intramuscularly - regularly intragluteally - while the patient is lying down, every two weeks. Normally the treatment is started with the administration of capsules 6X or 4X or with injection 6X. In case of absent or weak reactions the dosage may be gradually raised by shorter intervals - 2 ampules weekly at the most. In case of strong reactions, injections have to be discontinued; the treatment can be continued with the dosage form capsules. As a general advice the dosage has to be chosen adequately, so that strong general reactions do not occur and that the local reactions are confined to the site of injections. Fever, conditions of weakness. In cases of known hypersensitivity to Bacillus firmus, as a precaution, this preparation should not be administered. None known. Generally well tolerated. Occasionally local reactions like rubefaction, swelling or painfulness may be observed, normally vanishing without treatment. These effects are not to be seen as adverse reactions, but rather as an expression of effectiveness. In the first 2 or 3 days after the injection, sometimes conditions of weakness, fortified expectoration, slight painfulness of the region or subfebrile temperatures may occur. Strong general reactions are always a sign of overdosage or of incorrect injection technique. In this case the treatment can be continued orally with Recarcin capsules 6X or 4X.

Contraindications:

Adverse reactions:

229

Interactions with other remedies:

None known. An interval of four weeks should be kept to the administration of vaccinations. In cases of simultaneous treatment with immunosuppressive remedies, the effectiveness of Recarcin may be influenced. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. In isopathic therapy, Recarcin is employed for all chronic diseases as an unspecific irritative agent. The alternating administration of Recarcin and Utilin proved a success. Also, under the noticeable stimulus threshold a good effect of Recarcin is achieved. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

Side effects: Precautions:

Duration of treatment: Advice:

How supplied:

230

Recarcin 6X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Bacillus firmus extract 6X 1 ampule of 1 ml contains: Medically active substance: 1 ml Bacillus firmus 6X aqueous dilut. Other constituents: isotonic sodium chloride solution. Recarcin is a preparation from the Bacillus firmus, a particular strain from the group of non-pathogenic bacilli. Experience has shown that Recarcin raises the defensive capacity of a normal bacterial flora. Its content of polysaccharides, ferments, and specific protein combinations exerts a special effect of Recarcin that is to be understood in the sense of an immune- and irritative therapy. The progressing disease process is thereby blocked and the specific defense capacity is activated. In immunological test models, a significant rise in phagocytic activity has been established. A strong rise in the T-lymphocyte proliferation also confirms Recarcin as a potent immune modulator. All sub-acute and chronic inflammatory diseases, especially of the glands and serosae, arthritis and arthrosis, for immune modulation.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 1 ml to be injected deeply intramuscularly - regularly intragluteally - while the patient is lying down, every two weeks. Normally the treatment is started with the administration of capsules 6X or 4X. In case of absent or weak reactions the dosage may be gradually raised by shorter intervals - 2 ampules weekly at the most and/or by the injection of strength 4X. In case of strong reactions, injections have to be discontinued; the treatment can be continued with the dosage form capsules. As a general advice the dosage has to be chosen adequately, so that strong general reactions do not occur and that the local reactions are confined to the site of injections. Fever, conditions of weakness. In cases of known hypersensitivity to Bacillus firmus, as a precaution, this preparation should not be administered. None known. Generally well tolerated. Occasionally local reactions like rubefaction, swelling or painfulness may be observed, normally vanishing without treatment. These effects are not to be seen as adverse reactions, but rather as an expression of effectiveness. In the first 2 or 3 days after the injection, sometimes conditions of weakness, fortified expectoration, slight painfulness of the region or subfebrile temperatures may occur. Strong general reactions are always a sign of overdosage or of incorrect injection technique. In this case the treatment can be continued orally with Recarcin capsules 6X or 4X.

Contraindications:

Adverse reactions:

231

Interactions with other remedies:

None known. An interval of four weeks should be kept to the administration of vaccinations. In cases of simultaneous treatment with immunosuppressive remedies, the effectiveness of Recarcin may be influenced. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. In isopathic therapy, Recarcin is employed for all chronic diseases as an unspecific irritative agent. The alternating administration of Recarcin and Utilin proved a success. Also, under the noticeable stimulus threshold a good effect of Recarcin is achieved. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

Side effects: Precautions:

Duration of treatment: Advice:

How supplied:

232

Recarcin 4X
Capsules
For oral intake

Active ingredient: Composition:

Bacillus firmus extract 4X 1 capsule contains: Medically active substance: 330 mg Bacillus firmus 4X trit. Other constituents: lactose, hypromellosis (capsule shell). Recarcin is a preparation from the Bacillus firmus, a particular strain from the group of non-pathogenic bacilli. Experience has shown that Recarcin raises the defensive capacity of a normal bacterial flora. Its content of polysaccharides, ferments, and specific protein combinations exerts a special effect of Recarcin that is to be understood in the sense of an immune- and irritative therapy. The progressing disease process is thereby blocked and the specific defense capacity is activated. In immunological test models, a significant rise in phagocytic activity has been established. A strong rise in the T-lymphocyte proliferation also confirms Recarcin as a potent immune modulator. All sub-acute and chronic inflammatory diseases, especially of the glands and serosae, arthritis and arthrosis, for immune modulation.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1-2x weekly 1 capsule at bedtime, taken with some liquid. In cases of known hypersensitivity to Bacillus firmus, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Recarcin, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

233

Advice:

In isopathic therapy, Recarcin is employed for all chronic diseases as an unspecific irritative agent. The alternating administration of Recarcin and Utilin proved a success. Also, under the noticeable stimulus threshold a good effect of Recarcin is achieved. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

How supplied:

234

Recarcin 6X
Capsules
For oral intake

Active ingredient: Composition:

Bacillus firmus extract 6X 1 capsule contains: Medically active substance: 330 mg Bacillus firmus 6X trit. Other constituents: lactose, hypromellosis (capsule shell). Recarcin is a preparation from the Bacillus firmus, a particular strain from the group of non-pathogenic bacilli. Experience has shown that Recarcin raises the defensive capacity of a normal bacterial flora. Its content of polysaccharides, ferments, and specific protein combinations exerts a special effect of Recarcin that is to be understood in the sense of an immune- and irritative therapy. The progressing disease process is thereby blocked and the specific defense capacity is activated. In immunological test models, a significant rise in phagocytic activity has been established. A strong rise in the T-lymphocyte proliferation also confirms Recarcin as a potent immune modulator. All sub-acute and chronic inflammatory diseases, especially of the glands and serosae, arthritis and arthrosis, for immune modulation.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1-2x weekly 1 capsule at bedtime, taken with some liquid. In cases of known hypersensitivity to Bacillus firmus, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Recarcin, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

235

Advice:

In isopathic therapy, Recarcin is employed for all chronic diseases as an unspecific irritative agent. The alternating administration of Recarcin and Utilin proved a success. Also, under the noticeable stimulus threshold a good effect of Recarcin is achieved. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

How supplied:

236

Recarcin 6X
Suppositories

Active ingredient: Composition:

Bacillus firmus extract 6X 1 suppository contains: Medically active substance: 0.2 g Bacillus firmus 6X trit. Other constituents: hard fat, lactose. Recarcin is a preparation from the Bacillus firmus, a particular strain from the group of non-pathogenic bacilli. Experience has shown that Recarcin raises the defensive capacity of a normal bacterial flora. Its content of polysaccharides, ferments, and specific protein combinations exerts a special effect of Recarcin that is to be understood in the sense of an immune- and irritative therapy. The progressing disease process is thereby blocked and the specific defense capacity is activated. In immunological test models, a significant rise in phagocytic activity has been established. A strong rise in the T-lymphocyte proliferation also confirms Recarcin as a potent immune modulator. All sub-acute and chronic inflammatory diseases, especially of the glands and serosae, arthritis and arthrosis, for immune modulation.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 - 3 x weekly 1 suppository, inserted into the rectum at bedtime. In cases of known hypersensitivity to Bacillus firmus, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Recarcin, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

237

Advice:

In isopathic therapy, Recarcin is employed for all chronic diseases as an unspecific irritative agent. The alternating administration of Recarcin and Utilin proved a success. Also, under the noticeable stimulus threshold a good effect of Recarcin is achieved. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

How supplied:

238

Relivora Complex
Drops
Liquid dilution for oral intake

Active ingredients:

Drosera rotundifolia extract 3X, Echinacea angustifolia extract 2X, Juglans regia extract 4X 1 ml liquid dilution contains: Medically active substance: 25 l Drosera rotundifolia 3X dil., 2.5 l Echinacea angustifolia 2X dil., 250 l Juglans regia 4X dil. Other constituents: purified water, ethanol. Relivora Complex is a new type of combination homeopathic remedy including long proven effective substances. The individual constituents are perfectly matched in their concentrations in order to reach maximum synergistic effect. The individual components of Relivora Complex have the following significance: Extracts from Drosera rotundifolia act broncholytic, secretolytic and spasmolytic. The medical application of Echinacea angustifolia is indicated and proven for enhancing non specific defense capabilities in cases of resistance to antibiotics, recurring infections and inflammatory processes in the area of the urogenital system, the cervix-nose-ear-area and dermatology. Juglans regia, being an antiscrofulosum, is included for its high content in tannin. It is predominantly used externally for skin disorders such as acne, eczema, pyodermia and ulcers. The volatile oil acts antifungally, whilst the watery extract shows antiviral effects in tissue cultures. Relivora Complex is a unique and well balanced combination of naphthoquinone containing Drosera and Juglans with the immune stimulating factors of Echinacea. Stimulation of endogenic defensive capacities, in feverish processes, inflammatory processes of the pulmonary tract (hard, dry cough), bronchitis, whooping cough. Unless otherwise prescribed: 3 x daily 20-25 drops, undiluted. In case of acute conditions: 15 drops every two hours up to 6 x daily. This preparation should not be administered if cases of hypersensitivity against any of the ingredients, exipients or compositae are known. Furthermore, it should not be administered with progressive systemic diseases such as tuberculosis, leucosis, collagenosis, multiple sclerosis, AIDS, HIV infections and other auto-immune diseases. None known. Because of specific organic components of Relivora Complex, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Composition:

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies:

None known.

239

Side effects: Precautions:

None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The preparation contains 28 % (v/v) alcohol (ethanol). The following dosage forms are available: 30 ml and 100 ml dropper bottle 3X/2X/4X, 2 ml ampule 10 and 50 3X/4X/4X.

Duration of treatment: Advice: How supplied:

240

Relivora Complex
Ampules
Liquid dilution for injection

Active ingredients:

Drosera rotundifolia extract 3X, Echinacea angustifolia extract 4X, Juglans regia extract 4X 1 ampule of 2 ml contains: Medically active substance: 50.0 l Drosera rotundifolia 3X aqueous dilut., 500 l Echinacea angustifolia 4X aqueous dilut., 500 l Juglans regia 4X aqueous dilut. Other constituents: isotonic sodium chloride solution. Relivora Complex is a new type of combination homeopathic remedy including long proven effective substances. The individual constituents are perfectly matched in their concentrations in order to reach maximum synergistic effect. The individual components of Relivora Complex have the following significance: Extracts from Drosera rotundifolia act broncholytic, secretolytic and spasmolytic. The medical application of Echinacea angustifolia is indicated and proven for enhancing non specific defense capabilities in cases of resistance to antibiotics, recurring infections and inflammatory processes in the area of the urogenital system, the cervix-nose-ear-area and dermatology. Juglans regia, being an antiscrofulosum, is included for its high content in tannin. It is predominantly used externally for skin disorders such as acne, eczema, pyodermia and ulcers. The volatile oil acts antifungally, whilst the watery extract shows antiviral effects in tissue cultures. Relivora Complex is a unique and well balanced combination of naphthoquinone containing Drosera and Juglans with the immune stimulating factors of Echinacea. Stimulation of endogenic defensive capacities, in feverish processes, inflammatory processes of the pulmonary tract (hard, dry cough), bronchitis, whooping cough. Unless otherwise prescribed: 1 ampule of 2 ml to be injected either intramuscularly, subcutaneously, intracutaneously or intravenously, 1 x daily. This preparation should not be administered if cases of hypersensitivity against any of the ingredients, exipients or compositae are known. Furthermore, it should not be administered with progressive systemic diseases such as tuberculosis, leucosis, collagenosis, multiple sclerosis, AIDS, HIV infections and other auto-immune diseases. None known. In rare cases hypersensitivity reactions may occur. Preparations out of Echinacea were observed to cause skin rash, pruritus, rarely swelling of the face, shortness of breath, vertigo, or a decrease of blood pressure.

Composition:

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

241

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 30 and 100 ml dropper bottle 3X/2X/4X, 2 ml ampule 10 and 50 3X/4X/4X.

Duration of treatment: How supplied:

242

Ruberkehl 5X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Aspergillus ruber extract 5X 1 ml liquid dilution contains: Medically active substance: 1 ml Aspergillus ruber 5X dil. Other constituents: purified water. Clinical studies with Ruberkehl, a homeopathic preparation from Aspergillus ruber, have shown significant improvements in all relevant symptoms of acute allergic rhinitis. During therapy with Ruberkehl, the formation of Thelper cells, which are important for immune modulation, is raised. In these studies, it has been proven that due to the anti-allergic effect of Ruberkehl, any supplementary anti-allergic and symptomatically acting medication, could be significantly lowered. All chronic diseases of the upper and lower respiratory tract such as rhinitis, sinusitis, bronchitis, conjunctivitis (red, itching eyes), cystitis, nephritis.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops before a meal. For rubbing in: 1 x daily 5-10 drops at the location of the disease or into the bend of the elbow. In case of simultaneous treatment with injections, rub in 2 x weekly 5-10 drops on injection-free days. In cases of known hypersensitivity to Aspergillus ruber, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Ruberkehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X.

Duration of treatment: How supplied:

243

Ruberkehl 5X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Aspergillus ruber extract 5X 1 ampule of 1 ml contains: Medically active substance: 1 ml Aspergillus ruber 5X aqueous dilut. Other constituents: isotonic sodium chloride solution. Clinical studies with Ruberkehl, a homeopathic preparation from Aspergillus ruber, have shown significant improvements in all relevant symptoms of acute allergic rhinitis. During therapy with Ruberkehl, the formation of Thelper cells, which are important for immune modulation, is raised. In these studies, it has been proven that due to the anti-allergic effect of Ruberkehl, any supplementary anti-allergic and symptomatically acting medication, could be significantly lowered. All chronic diseases of the upper and lower respiratory tract such as rhinitis, sinusitis, bronchitis, conjunctivitis (red, itching eyes), cystitis, nephritis.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 1 ml to be injected either intramuscularly, subcutaneously, intracutaneously or intravenously, 2 x weekly. In cases of known hypersensitivity to Aspergillus ruber, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Ruberkehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X.

Duration of treatment: How supplied:

244

Ruberkehl 3X
Suppositories

Active ingredient: Composition:

Aspergillus ruber extract 3X 1 suppository contains: Medically active substance: 0.2 g Aspergillus ruber 3X trit. Other constituents: hard fat, lactose. Clinical studies with Ruberkehl, a homeopathic preparation from Aspergillus ruber, have shown significant improvements in all relevant symptoms of acute allergic rhinitis. During therapy with Ruberkehl, the formation of Thelper cells, which are important for immune modulation, is raised. In these studies, it has been proven that due to the anti-allergic effect of Ruberkehl, any supplementary anti-allergic and symptomatically acting medication, could be significantly lowered. All chronic diseases of the upper and lower respiratory tract such as rhinitis, sinusitis, bronchitis, conjunctivitis (red, itching eyes), cystitis, nephritis.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally at bedtime. In cases of known hypersensitivity to Aspergillus ruber, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Ruberkehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 3X.

Duration of treatment: How supplied:

245

Sankombi 5X
Drops
Liquid dilution for oral intake, rubbing in, inhalation

Active ingredients: Composition:

Mucor racemosus extract 5X, Aspergillus niger extract 5X 1 ml liquid dilution contains: Medically active substance: 0.5 ml Mucor racemosus 5X dil., 0.5 ml Aspergillus niger 5X dil. Other constituents: purified water. In the blood and tissue of humans and animals, live microbes which are normally harmless and which maintain diverse regulatory mechanisms. According to Prof. Enderlein, these endobionts are usually non-pathogenic phases of the mold fungi Mucor racemosus Fresen and Aspergillus niger van Tieghem. As all microbes, they are subject to the law of cyclogeny which means their development goes through the following series: primitive phase - bacterium - fungus whereby the virulence and pathogenicity of the endobiont increases with the rising development phase. If one supplies a sick organism stricken with higher valences with certain lower phase valences, these will be able to degrade the pathogenic forms into the inactive primitive stages by copulation with them. These can then be eliminated through the urinary paths, intestine, skin, and bronchi. Sankombi is a combination of these two fungal species, Mucor racemosus and Aspergillus niger. The effect of Sankombi on the T-cells which produce neopterin has been proven in clinical tests with children susceptible to infections. Neopterin is a messenger-substance which raises the immunity through activating the macrophages. The therapy with Sankombi improves both clinical complaints and serologic parameters. With the aid of this biological therapy, not only are mucosa and bacterial flora regulated, also the eliminative transport of metabolic products via lymph and blood is activated. Adenoiditis, swelling of the lymph nodes, Vincents angina, tonsillitis, a pediatrically suitable remedy for the re-establishment of symbiosis when there is a susceptibility for infections and allergies. Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops before a meal. For rubbing in: 1 x daily 5-10 drops at the location of the disease or into the bend of the elbow. In case of simultaneous treatment with injections, rub in 2 x weekly 5-10 drops on injection-free days. For inhalation: 10-20 drops, inhaled deeply 2-3 x daily. In cases of known hypersensitivity to Mucor racemosus or Aspergillus niger, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sankombi, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

246

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. In isopathic therapy, Sankombi is employed in the treatment of all chronic diseases based on an impairment of endobiosis. This can be caused by blockages as well as paratuberculosis. The following dosage form is available: 10 ml dropper bottle 5X.

Duration of treatment: Advice:

How supplied:

247

Sanoryzae 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Aspergillus oryzae extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Aspergillus oryzae 6X dil. Other constituents: purified water. Sanoryzae mainly acts on the vascular system by stimulating blood circulation. The remedy develops a rapid effectiveness particularly with disturbed coronary circulation, internal ear, as well as headaches resulting from disturbed circulation. Due to its circulatory regulating properties, Sanoryzae can be administered for high blood pressure. Coronary heart diseases, angina pectoris, for migraine conditioned by the circulatory system.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops before a meal. For rubbing in: 1 x daily 5-10 drops at the location of the disease or into the bend of the elbow. In case of simultaneous treatment with injections, rub in 2 x weekly 5-10 drops on injection-free days. In cases of known hypersensitivity to Aspergillus oryzae, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanoryzae, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X.

Duration of treatment: How supplied:

248

Sanukehl Acne 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Propionibacterium acnes extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Propionibacterium acnes 6X dil. Other constituents: purified water. Sanukehl Acne contains specific extracts of polysaccharide components (haptens) of Propionibacterium acnes which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Acne conglobata, rheumatoid arthritis.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For oral intake: In case of acute conditions: 5-10 drops every 12-24 hours. In case of chronic forms: 10 drops every 48 hours. For rubbing in: Every 1-2 days, use 5-10 drops at the location of the disease or into the bend of the elbow. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Propionibacterium acnes, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Acne, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Acne. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 5X.

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

Duration of treatment: How supplied:

249

Sanukehl Acne 5X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Propionibacterium acnes extract 5X 1 ampule of 1 ml contains: Medically active substance: 1 ml Propionibacterium acnes 5X aqueous dilut. Other constituents: isotonic sodium chloride solution. Sanukehl Acne contains specific extracts of polysaccharide components (haptens) of Propionibacterium acnes which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Acne conglobata, rheumatoid arthritis.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 1 ml to be injected deep intramuscularly or subcutaneously, every 1-3 days. In case of strong reactions, injections are to be discontinued; the treatment can be continued with drops. As a general recommendation, the dosage has to be chosen carefully, so that strong reactions do not occur and local reactions are confined to the site of injections. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Propionibacterium acnes, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Acne, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Acne. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

250

Duration of treatment: How supplied:

Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 5X.

251

Sanukehl Brucel 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Brucella melitensis extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Brucella melitensis 6X dil. Other constituents: purified water. Sanukehl Brucel contains specific extracts of polysaccharide components (haptens) of the Brucella melitensis which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Dysmenorrhoea, intermittent fever with influenza symptoms, myalgia subacute polyarthritis.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For oral intake: In case of acute conditions: 5-10 drops every 12-24 hours. In case of chronic forms: 10 drops every 48 hours. For rubbing in: Every 1-2 days, use 5-10 drops at the location of the disease or into the bend of the elbow. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Brucella melitensis, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Brucel, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Brucel. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 6X.

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

Duration of treatment: How supplied:

252

Sanukehl Brucel 6X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Brucella melitensis extract 6X 1 ampule of 1 ml contains: Medically active substance: 1 ml Brucella melitensis 6X aqueous dilut. Other constituents: isotonic sodium chloride solution. Sanukehl Brucel contains specific extracts of polysaccharide components (haptens) of the Brucella melitensis which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Dysmenorrhoea, intermittent fever with influenza symptoms, myalgia, subacute polyarthritis.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 1 ml to be injected deep intramuscularly or subcutaneously, every 1-3 days. In case of strong reactions, injections are to be discontinued; the treatment can be continued with the drops. As a general recommendation, the dosage has to be chosen carefully, so that strong reactions do not occur and local reactions are confined to the site of injections. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Brucella melitensis, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Brucel, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Brucel. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

253

Duration of treatment: How supplied:

Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 6X.

254

Sanukehl Cand 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Candida albicans extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Candida albicans 6X dil. Other constituents: purified water. Sanukehl Cand is produced from the A and B serotypes of Candida albicans, to which by far most of the isolated human Candidiasis agents belong. Sanukehl Cand contains specific extracts of polysaccharide components (haptens) of Candida albicans which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Diseases of the mouth, like stomatitis, gingivitis, perlche, aphthae; spasmodic, painful colitis of the small and large intestine, obstipation after treatment with antibiotics, allergic asthma, vulvitis, vulvo vaginitis, kraurosis, rectilinear fissural eczema of wrinkles or mucosa, interdigital eczema of hands or feet, dermatosis after treatment with antibiotics. Unless otherwise prescribed: For oral intake: In case of acute conditions: 5-10 drops every 12-24 hours. In case of chronic forms: 10 drops every 48 hours. For rubbing in: Every 1-2 days, use 5-10 drops at the location of the disease or into the bend of the elbow. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Candida albicans, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Cand, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Cand. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

255

Duration of treatment: How supplied:

Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 5X.

256

Sanukehl Cand 5X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Candida albicans extract 5X 1 ampule of 1 ml contains: Medically active substance: 1 ml Candida albicans 5X aqueous dilut. Other constituents: isotonic sodium chloride solution. Sanukehl Cand is produced from the A and B serotypes of Candida albicans, to which by far most of the isolated human Candidiasis agents belong. Sanukehl Cand contains specific extracts of polysaccharide components (haptens) of Candida albicans which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Diseases of the mouth, like stomatitis, gingivitis, perlche, aphthae, spasmodic, painful colitis of the small and large intestine, obstipation after treatment with antibiotics, allergic asthma, vulvitis, vulvo vaginitis, kraurosis, rectilinear fissural eczema of wrinkles or mucosa, interdigital eczema of hands or feet, dermatosis after treatment with antibiotics. Unless otherwise prescribed: 1 ampule of 1 ml to be injected deep intramuscularly or subcutaneously, every 1-3 days. In case of strong reactions, injections are to be discontinued; the treatment can be continued with the drops. As a general recommendation, the dosage has to be chosen carefully, so that strong reactions do not occur and local reactions are confined to the site of injections. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Candida albicans, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Cand, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Cand. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects:

257

Precautions:

As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 5X.

Duration of treatment: How supplied:

258

Sanukehl Coli 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Escherichia coli extract 6X 1 ml liquid dilution bottle contains: Medically active substance: 1 ml Escherichia coli 6X dil. Other constituents: purified water. Sanukehl Coli contains specific extracts of polysaccharide components (haptens) of Escherichia coli which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Cholangitis, cholecystitis, gastroenteritis, colitis, pyelonephritis, spermatocystitis, epididymitis, cystitis, prostatitis, salpingitis, metritis, vaginitis.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For oral intake: In case of acute conditions: 5-10 drops every 12-24 hours. In case of chronic forms: 10 drops every 48 hours. For rubbing in: Every 1-2 days, use 5-10 drops at the location of the disease or into the bend of the elbow. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Escherichia coli, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Coli, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Coli. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 7X.

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

Duration of treatment: How supplied:

259

Sanukehl Coli 7X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Escherichia coli extract 7X 1 ampule of 1 ml contains: Medically active substance: 1 ml Escherichia coli 7X aqueous dilut. Other constituents: isotonic sodium chloride solution. Sanukehl Coli contains specific extracts of polysaccharide components (haptens) of Escherichia coli which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Cholangitis, cholecystitis, gastroenteritis, colitis, pyelonephritis, spermatocystitis, epididymitis, cystitis, prostatitis, salpingitis, metritis, vaginitis.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 1 ml to be injected deep intramuscularly or subcutaneously, every 1-3 days. In case of strong reactions, injections are to be discontinued; the treatment can be continued with the drops. As a general recommendation, the dosage has to be chosen carefully, so that strong reactions do not occur and local reactions are confined to the site of injections. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Escherichia coli, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Coli, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Coli. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

260

Duration of treatment: How supplied:

Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 7X.

261

Sanukehl Klebs 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Klebsiella pneumoniae extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Klebsiella pneumoniae 6X dil. Other constituents: purified water. Sanukehl Klebs contains specific extracts of polysaccharide components (haptens) of Klebsiella pneumoniae which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. As a supporting therapy during or after Friedlnders pneumonia, for silicosis, pneumoconiosis, bronchiectasis, bronchial asthma, as an adjuvant for acute influenza, pleurisy, pneumonia, for side effects caused by a therapy with antibiotics. Unless otherwise prescribed: For oral intake: In case of acute conditions: 5-10 drops every 12-24 hours. In case of chronic forms: 10 drops every 48 hours. For rubbing in: Every 1-2 days, use 5-10 drops at the location of the disease or into the bend of the elbow. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Klebsiella pneumoniae, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Klebs, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Klebs. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 6X.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

Duration of treatment: How supplied:

262

Sanukehl Klebs 6X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Klebsiella pneumoniae extract 6X 1 ampule of 1 ml contains: Medically active substance: 1 ml Klebsiella pneumoniae 6X aqueous dilut. Other constituents: isotonic sodium chloride solution. Sanukehl Klebs contains specific extracts of polysaccharide components (haptens) of Klebsiella pneumoniae which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. As a supporting therapy during or after Friedlnders pneumonia, for silicosis, pneumoconiosis, bronchiectasis, bronchial asthma, as an adjuvant for acute influenza, pleurisy, pneumonia, for side effects caused by a therapy with antibiotics. Unless otherwise prescribed: 1 ampule of 1 ml to be injected deep intramuscularly or subcutaneously, every 1-3 days. In case of strong reactions, injections are to be discontinued; the treatment can be continued with the drops. As a general recommendation, the dosage has to be chosen carefully, so that strong reactions do not occur and local reactions are confined to the site of injections. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Klebsiella pneumoniae, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Klebs, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Klebs. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

263

Duration of treatment: How supplied:

Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 6X.

264

Sanukehl Myc 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Mycobacterium bovis extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Mycobacterium bovis 6X dil. Other constituents: purified water. Sanukehl Myc contains specific extracts of polysaccharide components (haptens) of Mycobacterium bovis which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Bronchial asthma, pleurisy, rhinitis, arthritis, osteochondrosis, juvenile acne, eczema with fissures, psoriasis, lupus erythematosus, urticaria, conjunctivitis, hordeolum, keratitis, ventricular and duodenal ulcer, enterocolitis, aphonia, laryngeal ulceration, arrhythmia, cardialgia, nephritis, cystitis, cholecystitis, otitis, headache, metritis, hydrocele. Unless otherwise prescribed: For oral intake: In case of acute conditions: 5-10 drops every 12-24 hours. In case of chronic forms: 10 drops every 48 hours. For rubbing in: Every 1-2 days, use 5-10 drops at the location of the disease or into the bend of the elbow. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Mycobacterium bovis, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Myc, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Myc. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

265

Duration of treatment: How supplied:

Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 5X.

266

Sanukehl Myc 5X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Mycobacterium bovis extract 5X 1 ampule of 1 ml contains: Medically active substance: 1 ml Mycobacterium bovis 5X aqueous dilut. Other constituents: isotonic sodium chloride solution. Sanukehl Myc contains specific extracts of polysaccharide components (haptens) of Mycobacterium bovis which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Bronchial asthma, pleurisy, rhinitis, arthritis, osteochondrosis, juvenile acne, eczema with fissures, psoriasis, lupus erythematosus, urticaria, conjunctivitis, hordeolum, keratitis, ventricular and duodenal ulcer, enterocolitis, aphonia, laryngeal ulceration, arrhythmia, cardialgia, nephritis, cystitis, cholecystitis, otitis, headache, metritis, hydrocele. Unless otherwise prescribed: 1 ampule of 1 ml to be injected deep intramuscularly or subcutaneously, every 1-3 days. In case of strong reactions, injections are to be discontinued; the treatment can be continued with the drops. As a general recommendation, the dosage has to be chosen carefully, so that strong reactions do not occur and local reactions are confined to the site of injections. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Mycobacterium bovis, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Myc, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Myc. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects:

267

Precautions:

As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 5X.

Duration of treatment: How supplied:

268

Sanukehl Prot 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Proteus vulgaris extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Proteus vulgaris 6X dil. Other constituents: purified water. Sanukehl Prot contains specific extracts of polysaccharide components (haptens) of Proteus vulgaris which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Gastroenteritis (especially diarrhea of infants), peritonitis, cystopyelitis, puerperal sepsis, otitis, gangrenous pulmonary involvement, osteomyelitis, intestinal dysbiosis after treatment with antibiotics, disturbed peripheral circulation, ventricular and duodenal ulcer, hematemesis, angioneurotic edemas, Menires disease, herpes. Unless otherwise prescribed: For oral intake: In case of acute conditions: 5-10 drops every 12-24 hours. In case of chronic forms: 10 drops every 48 hours. For rubbing in: Every 1-2 days, use 5-10 drops at the location of the disease or into the bend of the elbow. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Proteus vulgaris, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Prot, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Prot. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

269

Duration of treatment: How supplied:

Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 7X.

270

Sanukehl Prot 7X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Proteus vulgaris extract 7X 1 ampule of 1 ml contains: Medically active substance: 1 ml Proteus vulgaris 7X aqueous dilut. Other constituents: isotonic sodium chloride solution. Sanukehl Prot contains specific extracts of polysaccharide components (haptens) of Proteus vulgaris which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Gastroenteritis (especially diarrhea of infants), peritonitis, cystopyelitis, puerperal sepsis, otitis, gangrenous pulmonary involvement, osteomyelitis, intestinal dysbiosis after treatment with antibiotics, disturbed peripheral circulation, ventricular and duodenal ulcer, hematemesis, angioneurotic edemas, Menires disease, herpes. Unless otherwise prescribed: 1 ampule of 1 ml to be injected deep intramuscularly or subcutaneously, every 1-3 days. In case of strong reactions, injections are to be discontinued; the treatment can be continued with the drops. As a general recommendation, the dosage has to be chosen carefully, so that strong reactions do not occur and local reactions are confined to the site of injections. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Proteus vulgaris, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Prot, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Prot. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

271

Duration of treatment: How supplied:

Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 7X.

272

Sanukehl Pseu 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Pseudomonas aeruginosa extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Pseudomonas aeruginosa 6X dil. Other constituents: purified water. Sanukehl Pseu contains specific extracts of polysaccharide components (haptens) of Pseusomonas aeruginosa which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Infectious and allergic dermatitis, pruritus, angioneurotic edema, collagenosis, fibromyalgia, ulcer cruris, keloids, burns, bronchial asthma, sinusitis, pharyngitis, chronic bronchitis, hay-fever, otitis, autoimmune diseases, treatment of complaints caused by an immunosuppressive treatment. Unless otherwise prescribed: For oral intake: In case of acute conditions: 5-10 drops every 12-24 hours. In case of chronic forms: 10 drops every 48 hours. For rubbing in: Every 1-2 days, use 5-10 drops at the location of the disease or into the bend of the elbow. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Pseudomonas aeruginosa, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Pseu, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Pseu. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 5X.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

Duration of treatment: How supplied:

273

Sanukehl Pseu 5X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Pseudomonas aeruginosa extract 5X 1 ampule of 1 ml contains: Medically active substance: 1 ml Pseudomonas aeruginosa 5X aqueous dilut. Other constituents: isotonic sodium chloride solution. Sanukehl Pseu contains specific extracts of polysaccharide components (haptens) of Pseusomonas aeruginosa which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Infectious and allergic dermatitis, pruritus, angioneurotic edema, collagenosis, fibromyalgia, ulcer cruris, keloids, burns, bronchial asthma, sinusitis, pharyngitis, chronic bronchitis, hay-fever, otitis, autoimmune diseases, treatment of complaints caused by an immunosuppressive treatment. Unless otherwise prescribed: 1 ampule of 1 ml to be injected deep intramuscularly or subcutaneously, every 1-3 days. In case of strong reactions, injections are to be discontinued; the treatment can be continued with drops. As a general recommendation, the dosage has to be chosen carefully, so that strong reactions do not occur and local reactions are confined to the site of injections. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Pseudomonas aeruginosa, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Pseu, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Pseu. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

274

Duration of treatment: Advice: How supplied:

Dependent on the advice of the physician or health care professional. In some countries this preparation is only available in potency 6X. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 5X (6X).

275

Sanukehl Salm 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Salmonella enteriditis extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Salmonella enteriditis 6X dil. Other constituents: purified water. Sanukehl Salm contains specific extracts of polysaccharide components (haptens) of Salmonella enteriditis which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Impaired development, malnutrition of children, chronic pancreatitis, enterobiasis (oxyuriasis), chronic gastroenteritis, celiac disease, furunculosis, rheumatic fever. Unless otherwise prescribed: For oral intake: In case of acute conditions: 5-10 drops every 12-24 hours. In case of chronic forms: 10 drops every 48 hours. For rubbing in: Every 1-2 days, use 5-10 drops at the location of the disease or into the bend of the elbow. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Salmonella enteriditis, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Salm, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Salm. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 6X.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

Duration of treatment: How supplied:

276

Sanukehl Salm 6X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Salmonella enteriditis extract 6X 1 ampule of 1 ml contains: Medically active substance: 1 ml Salmonella enteriditis 6X aqueous dilut. Other constituents: isotonic sodium chloride solution. Sanukehl Salm contains specific extracts of polysaccharide components (haptens) of Salmonella enteriditis which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Impaired development, malnutrition of children, chronic pancreatitis, enterobiasis (oxyuriasis), chronic gastroenteritis, celiac disease, furunculosis, rheumatic fever. Unless otherwise prescribed: 1 ampule of 1 ml to be injected deep intramuscularly or subcutaneously, every 1-3 days. In case of strong reactions, injections are to be discontinued; the treatment can be continued with the drops. As a general recommendation, the dosage has to be chosen carefully, so that strong reactions do not occur and local reactions are confined to the site of injections. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Salmonella enteriditis, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Salm, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Salm. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

277

Duration of treatment: How supplied:

Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 6X.

278

Sanukehl Serra 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Serratia marcescens extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Serratia marcescens 6X dil. Other constituents: purified water. Sanukehl Serra contains specific extracts of polysaccharide components (haptens) of Serratia marcescens which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Nosocomial infections with Serratia marcescens.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For oral intake: In case of acute conditions: 5-10 drops every 12-24 hours. In case of chronic forms: 10 drops every 48 hours. For rubbing in: Every 1-2 days, use 5-10 drops at the location of the disease or into the bend of the elbow. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Serratia marcescens, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Serra, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Serra. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 5X.

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

Duration of treatment: How supplied:

279

Sanukehl Serra 5X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Serratia marcescens extract 5X 1 ampule of 1 ml contains: Medically active substance: 1 ml Serratia marcescens 5X aqueous dilut. Other constituents: isotonic sodium chloride solution. Sanukehl Serra contains specific extracts of polysaccharide components (haptens) of Serratia marcescens which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Nosocomial infections with Serratia marcescens.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 1 ml to be injected deep intramuscularly or subcutaneously, every 1-3 days. In case of strong reactions, injections are to be discontinued; the treatment can be continued with drops. As a general recommendation, the dosage has to be chosen carefully, so that strong reactions do not occur and local reactions are confined to the site of injections. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Serratia marcescens, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Serra, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Serra. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

280

Duration of treatment: Advice: How supplied:

Dependent on the advice of the physician or health care professional. In some countries this preparation is only available in potency 7X. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 5X (7X).

281

Sanukehl Staph 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Staphylococcus aureus extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Staphylococcus aureus 6X dil. Other constituents: purified water. Sanukehl Staph contains specific extracts of polysaccharide components (haptens) of Staphylococcus aureus which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Folliculosis, furunculosis, impetigo, acne conglobata/necrotica, blepharitis, hordeolum, chalazion, pleuropneumonia, sinusitis, angina, nephritis, urogenital infections by staphylococci, endocarditis, meningitis, osteomyelitis, otitis, mastoiditis, anthrax. Unless otherwise prescribed: For oral intake: In case of acute conditions: 5-10 drops every 12-24 hours. In case of chronic forms: 10 drops every 48 hours. For rubbing in: Every 1-2 days, use 5-10 drops at the location of the disease or into the bend of the elbow. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Staphylococcus aureus, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Staph, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Staph. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 5X.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

Duration of treatment: How supplied:

282

Sanukehl Staph 5X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Staphylococcus aureus extract 5X 1 ampule of 1 ml contains: Medically active substance: 1 ml Staphylococcus aureus 5X aqueous dilut. Other constituents: isotonic sodium chloride solution. Sanukehl Staph contains specific extracts of polysaccharide components (haptens) of Staphylococcus aureus which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Folliculosis, furunculosis, impetigo, acne conglobata/necrotica, blepharitis, hordeolum, chalazion, pleuropneumonia, sinusitis, angina, nephritis, urogenital infections by staphylococci, endocarditis, meningitis, osteomyelitis, otitis, mastoiditis, anthrax. Unless otherwise prescribed: 1 ampule of 1 ml to be injected deep intramuscularly or subcutaneously, every 1-3 days. In case of strong reactions, injections are to be discontinued; the treatment can be continued with drops. As a general recommendation, the dosage has to be chosen carefully, so that strong reactions do not occur and local reactions are confined to the site of injections. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Staphylococcus aureus, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Staph, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Staph. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

283

Duration of treatment: How supplied:

Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 5X.

284

Sanukehl Strep 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Streptococcus pyogenes extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Streptococcus pyogenes 6X dil. Other constituents: purified water. Sanukehl Strep contains specific extracts of polysaccharide components (haptens) of Streptococcus pyogenes which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Alopecia, eczema, empyema, phlegmon, cardialgia, endo-, myo- and pericarditis, primary chronic polyarthritis, osteomyelitis, tonsillitis, otitis media, migraine, mastitis puerperal. Unless otherwise prescribed: For oral intake: In case of acute conditions: 5-10 drops every 12-24 hours. In case of chronic forms: 10 drops every 48 hours. For rubbing in: Every 1-2 days, use 5-10 drops at the location of the disease or into the bend of the elbow. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Streptococcus pyogenes, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Strep, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Strep. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 5X.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

Duration of treatment: How supplied:

285

Sanukehl Strep 5X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Streptococcus pyogenes extract 5X 1 ampule of 1 ml contains: Medically active substance: 1 ml Streptococcus pyogenes 5X aqueous dilut. Other constituents: isotonic sodium chloride solution. Sanukehl Strep contains specific extracts of polysaccharide components (haptens) of Streptococcus pyogenes which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Alopecia, eczema, empyema, phlegmon, cardialgia, endo-, myo- and pericarditis, primary chronic polyarthritis, osteomyelitis, tonsillitis, otitis media, migraine, mastitis puerperal. Unless otherwise prescribed: 1 ampule of 1 ml to be injected deep intramuscularly or subcutaneously, every 1-3 days. In case of strong reactions, injections are to be discontinued; the treatment can be continued with drops. As a general recommendation, the dosage has to be chosen carefully, so that strong reactions do not occur and local reactions are confined to the site of injections. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Streptococcus pyogenes, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Strep, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Strep. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

286

Duration of treatment: How supplied:

Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 5X.

287

Sanukehl Trich 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Trichophyton verrucosum extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Trichophyton verrucosum 6X dil. Other constituents: purified water. Sanukehl Trich contains specific extracts of polysaccharide components (haptens) of the Trichophyton verrucosum which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Mycosis of the hair, skin, nails, tinea, trichophytosis, impairment of skin function, hair loss.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For oral intake: In case of acute conditions: 510 drops every 12-24 hours. In case of chronic forms: 10 drops every 48 hours. For rubbing in: Every 1-2 days, use 5-10 drops at the location of the disease or into the bend of the elbow. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Trichophyton verrucosum, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Trich, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Trich. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 5X.

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

Duration of treatment: How supplied:

288

Sanukehl Trich 5X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Trichophyton verrucosum extract 5X 1 ampule of 1 ml contains: Medically active substance: 1 ml Trichophyton verrucosum 5X aqueous dilut. Other constituents: isotonic sodium chloride solution. Sanukehl Trich contains specific extracts of polysaccharide components (haptens) of the Trichophyton verrucosum which are often used as intermediate agents during treatment with the corresponding nosode. The effect is based on the absorption of the bacterial antigens and their toxins. Through the Sanukehl preparation, any intense initial deterioration or blockage of antigens is relieved or eliminated. Specific microbiological cleansing of the terrain is possible by the application of the Sanukehls. Mycosis of the hair, skin, nails, tinea, trichophytosis, impairment of skin function, hair loss.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 1 ml to be injected deep intramuscularly or subcutaneously, every 1-3 days. In case of strong reactions, injections are to be discontinued; the treatment can be continued with drops. As a general recommendation, the dosage has to be chosen carefully, so that strong reactions do not occur and local reactions are confined to the site of injections. After two months treatment the therapy should be interrupted for several months. In cases of known hypersensitivity to Trichophyton verrucosum, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Sanukehl Trich, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically. Immunosuppressive remedies or therapies may impair the effectiveness of Sanukehl Trich. An interval of four weeks before and after the treatment with oral administered vaccines must be employed. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

Contraindications:

Adverse reactions:

Interactions with other remedies:

Side effects: Precautions:

289

Duration of treatment: How supplied:

Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 6X, 1 ml ampule 10 and 50 5X.

290

Sanumgerman 6X
Drops
Liquid dilution for oral intake

Active ingredient: Composition:

Di-potassium-germanium(IV)-citrate-L(+)lactate 6X 100 ml dropper bottle contains: Medically active substance: 100 ml Dipotassium-germanium(IV)-citrate-L(+)lactate 6X dil. Other constituents: purified water, ethanol. Sanumgerman is an organic compound of germanium that positively influences growth and regulation of biological systems in vitro and in vivo. In the periodic system of the chemical elements, germanium belongs to the same main group as silicon, which explains its regulative ability.Experimental examinations have shown that germanium protects against oxidation to enzymes with SH-groups, resulting in an improvement of the defense against free radicals and peroxides. Because of its immunmodulatoric effect, organic germanium supports the formation of interferons as well as the activation of macrophages and natural killer cells. In animal experiments, its sedative effects on the central nervous system were also established. Peripheral arterial circulatory disorders, cerebrosclerosis, Raynauds disease, chronic rheumatism, Parkinsons disease, epilepsy, adjuvant therapy for cancer. Unless otherwise prescribed: For oral intake: 1-3 x daily 1-2 teaspoons before a meal. None known. None known.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications: Adverse reactions: Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The preparation contains 12.4% (v/v) alcohol (ethanol). The following dosage forms are available: 100 ml dropper bottle 6X.

Duration of treatment: Advice: How supplied:

291

Sanuvis 2X
Drops
Liquid dilution for oral intake

Active ingredient: Composition:

Acidum L(+)-lacticum 2X 1 ml liquid dilution contains: Medically active substance: 1 ml Acidum L(+)-lacticum 2X dil. Other constituents: purified water, ethanol. L(+)-lactic acid (Acidum L(+)-lacticum) is a natural substance which activates oxidation and cell regeneration. According to Dr. Seeger, it is capable of raising the cellular respiration in the mitochondria by 350%, especially when they have been damaged due to a damaged metabolism. When there is an acute cellular oxygen deficiency or an overburden with carbohydrates, lactic acid fermentation begins in these cells. The result is a toxic excess in levorotatory lactic acid which facilitates, along with other factors, excessive cell proliferation. Lactic acid, a substance for growth, in larger toxic amounts enhances proliferation which promotes the mitosis of the degenerated cells. Dextrorotary lactic acid in lower potencies is used for the development of a racemate and elimination. Lapse in the acid-base-equilibrium, acidification of blood and deacidification of tissue; metabolic disturbances mainly resulting from the increased production of levorotatory lactic acid e.g. diabetes, tissue degeneration and functional heart disorders; skin diseases such as psoriasis and ichthyosis Unless otherwise prescribed: 1-3 x daily 5 drops. None known. None known.

Characteristics:

According to experience, to be administered in cases of:

Application: Contraindications: Adverse reactions: Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

292

Advice:

Sanuvis can be administered as a basic therapeutic agent together with all mold and yeast preparations. The preparation contains 19 % (v/v) alcohol (ethanol). The following dosage forms are available: 30 ml dropper bottle 2X, 100 ml dropper bottle 4X/6X/12X/30X/200X potency mixture, 2 ml ampule 10 and 50 4X/6X/12X/30X/200X potency mixture, 80 tablets 4X/6X/12X/30X/200X potency mixture, 30 g tube of ointment 1X.

How supplied:

293

Sanuvis 4X/6X/12X/30X/200X
Drops
Liquid dilution for oral intake

Active ingredient: Composition:

Acidum L(+)-lacticum 4X/6X/12X/30X/200X 1 ml liquid dilution contains: Medically active substance: 0.2 ml Acidum L(+)-lacticum 4X dil., 0.2 ml Acidum L(+)-lacticum 6X dil., 0.2 ml Acidum L(+)-lacticum 12X dil., 0.2 ml Acidum L(+)-lacticum 30X dil., 0.2 ml Acidum L(+)-lacticum 200X dil. Other constituents: purified water, ethanol. L(+)-lactic acid (Acidum L(+)-lacticum) is a natural substance which activates oxidation and cellular regeneration. According to Dr. Seeger, it is capable of raising the cellular respiration in the mitochondria by 350 %, especially when they have been damaged due to a tumorous metabolism. When there is an acute cellular oxygen deficiency, lactic acid fermentation begins in these cells. The result is a toxic excess in lactic acid which facilitates, along with other factors, the degeneration of cells. Lactic acid, a substance for growth, in toxic amounts enhances proliferation. In isopathy, highly diluted dextrorotatory lactic acid is applied for regulation. By bringing together several potencies, as in Sanuvis potency accord, several phases of the metabolism can be simultaneously favorably affected. Regulation of the pH-value, pre-and post-operative therapy, metabolic disorders, for support of cancer treatment, chronic skin diseases and functional heart complaints, for support in gastrointestinal-hepatic disorders. Unless otherwise prescribed: 3 x daily 60 drops (approx. one teaspoon) before a meal. None known. None known.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications: Adverse reactions: Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

294

Advice:

Sanuvis can be administered as a basic therapeutic agent together with all mold and yeast preparations. The preparation contains 12.4 % (v/v) alcohol (ethanol). The following dosage forms are available: 30 ml dropper bottle 2X, 100 ml dropper bottle 4X/6X/12X/30X/200X potency mixture, 2 ml ampule 10 and 50 4X/6X/12X/30X/200X potency mixture, 80 tablets 4X/6X/12X/30X/200X potency mixture, 30 g tube of ointment 1X.

How supplied:

295

Sanuvis 4X/6X/12X/30X/200X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Acidum L(+)-lacticum 4X/6X/12X/30X/200X 1 ampule of 2 ml contains: Medically active substance: 0.4 ml Acidum L(+)-lacticum 4X aqueous dilut., 0.4 ml Acidum L(+)-lacticum 6X aqueous dilut., 0.4 ml Acidum L(+)-lacticum 12X aqueous dilut., 0.4 ml Acidum L(+)lacticum 30X aqueous dilut., 0.4 ml Acidum L(+)-lacticum 200X aqueous dilut. Other constituents: isotonic sodium chloride solution. L(+)-lactic acid (Acidum L(+)-lacticum) is a natural substance which activates oxidation and cellular regeneration. According to Dr. Seeger, it is capable of raising the cellular respiration in the mitochondria by 350 %, especially when they have been damaged due to a tumorous metabolism. When there is an acute cellular oxygen deficiency, lactic acid fermentation begins in these cells. The result is a toxic excess in lactic acid which facilitates, along with other factors, the degeneration of cells. Lactic acid, a substance for growth, in toxic amounts enhances proliferation. In isopathy, highly diluted dextrorotatory lactic acid is applied for regulation. By bringing together several potencies, as in Sanuvis potency accord, several phases of the metabolism can be simultaneously favorably affected. Regulation of the pH-value, pre-and post-operative therapy, metabolic disorders, for support of cancer treatment, chronic skin diseases and functional heart complaints, for support in gastrointestinal-hepatic disorders. Unless otherwise prescribed: 1 ampule of 2 ml to be injected intramuscularly, 1-3 x weekly. None known. None known.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications: Adverse reactions: Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

296

Advice:

Sanuvis can be administered as a basic therapeutic agent together with all mold and yeast preparations. In isopathic therapy, Sanuvis is employed as an adjuvant for the parenteral administration of Mucokehl. The following dosage forms are available: 30 ml dropper bottle 2X, 100 ml dropper bottle 4X/6X/12X/30X/200X potency mixture, 2 ml ampule 10 and 50 4X/6X/12X/30X/200X potency mixture, 80 tablets 4X/6X/12X/30X/200X potency mixture, 30 g tube of ointment 1X.

How supplied:

297

Sanuvis 4X/6X/12X/30X/200X
Tablets

Active ingredient: Composition:

Acidum L(+)-lacticum 4X/6X/12X/30X/200X 1 tablet contains: Medically active substance: 50 mg Acidum L(+)-lacticum 4X trit., 50 mg Acidum L(+)-lacticum 6X trit., 50 mg Acidum L(+)-lacticum 12X trit., 50 mg Acidum L(+)-lacticum 30X trit., 50 mg Acidum L(+)-lacticum 200X trit. Other constituents: lactose, potato starch, magnesium stearate. L(+)-lactic acid (Acidum L(+)-lacticum) is a natural substance which activates oxidation and cellular regeneration. According to Dr. Seeger, it is capable of raising the cellular respiration in the mitochondria by 350 %, especially when they have been damaged due to a tumorous metabolism. When there is an acute cellular oxygen deficiency, lactic acid fermentation begins in these cells. The result is a toxic excess in lactic acid which facilitates, along with other factors, the degeneration of cells. Lactic acid, a substance for growth, in toxic amounts enhances proliferation. In isopathy, highly diluted dextrorotatory lactic acid is applied for regulation. By bringing together several potencies, as in Sanuvis potency accord, several phases of the metabolism can be simultaneously favorably affected. Regulation of the pH-value, pre-and post-operative therapy, metabolic disorders, for support of cancer treatment, chronic skin diseases and functional heart complaints, for support in gastrointestinal-hepatic disorders. Unless otherwise prescribed: children: 1-3 x daily 1 tablet, adults: 2-3 x daily 3 tablets. None known. None known.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications: Adverse reactions: Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

298

Advice:

Sanuvis can be administered as a basic therapeutic agent together with all mold and yeast preparations. The following dosage forms are available: 30 ml dropper bottle 2X, 100 ml dropper bottle 4X/6X/12X/30X/200X potency mixture, 2 ml ampule 10 and 50 4X/6X/12X/30X/200X potency mixture, 80 tablets 4X/6X/12X/30X/200X potency mixture, 30 g tube of ointment 1X.

How supplied:

299

Sanuvis 1X
Ointment

Active ingredient: Composition:

Acidum L(+)-lacticum 1X 1 g ointment contains: Medically active substance: 0.1 g Acidum L(+)-lacticum 1X dil. Other constituents: 0.38 g Lanolin alcohols ointment, 0.1 g Coconut oil fract., 0.03 g Glyceryl monostearate 40-50%, 0.23 g Propylene glycol, 0.02 g Magnesium sulphate x 7 H2O, 0.14g water for injection. The human skins acid coating provides effective protection from numerous external influences. The skin is the bodys largest organ and becomes frequently damaged through repeated use of cleansing products i.e. soaps, shower gels, lotions etc., which often shows itself in the alkaline reaction in sick people. The result is a disturbed acid coating which renders one vulnerable to attacks by pathogenic micro-organisms and environmental toxins. The skin has a considerable physiologic capacity for storing dextrorotatory lactic acid (Acidum L(+)-lacticum). Sanuvis ointment with its active substance Acidum L(+)-lacticum regenerates the acid coating of the skin, which is a precondition for successfully treating the most diverse skin diseases. Moreover, dextrorotatory lactic acid is, in itself, a natural substance that activates cellular regeneration whereby it raises cellular respiration in the mitochondria and in this way initiates healing processes. Cosmetically, Sanuvis ointment is applied for the common problem of dry skin and its concomitant early aging and wrinkling. Regulation of the pH-value, especially for chronic skin diseases as psoriasis, ichthyosis, rhagades.

Characteristics:

According to experience, to be administered in cases of: Application: Contraindications: Adverse reactions: Interactions with other remedies: Side effects: Precautions:

Unless otherwise prescribed: Apply on the affected area 1 to 3 x daily. None known. None known.

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

300

Advice:

Sanuvis can be administered as a basic therapeutic agent together with all mold and yeast preparations. The following dosage forms are available: 30 ml dropper bottle 2X, 100 ml dropper bottle 4X/6X/12X/30X/200X potency mixture, 2 ml ampule 10 and 50 4X/6X/12X/30X/200X potency mixture, 80 tablets 4X/6X/12X/30X/200X potency mixture, 30 g tube of ointment 1X.

How supplied:

301

Selenokehl 4X
Drops
Liquid dilution for oral intake

Active ingredient: Composition:

Sodium selenite 4X 10 ml dropper bottle contains: Medically active substance: 0.8 ml Sodium selenite 4X dil. Other constituents: purified water, ethanol. Selenium is an essential trace element. In the human body it is chiefly connected with the enzyme glutathione peroxidase which is a constituent of the antioxidative protective system of the cell. In test models it has been proven that the selenium-containing glutathione peroxidase is one of the strongest, most effective enzymes of the body for absorbing radicals. Among other benefits, it lowers the rate of peroxidation of lipids and thereby protects the cellular membrane from damages. Deficiency in selenium increases the toxicity of heavy metals such as mercury, lead and cadmium, and also it potentizes weakness of the liver that is due to oxidative and chemical influences. The significance of selenium as an antioxidant, also its anti-carcinogenic and anti-mutagenic properties, have been well researched. It has been proven in numerous tests that a continuing intake of selenium can inhibit chemically and virally induced tumorous developments. This is valid especially for tumorous systems such as skin, liver, intestinal and breast cancer. Selenium deficiency due to malnutrition and malabsorption, for amalgam detoxification.

Characteristics:

According to experience, to be administered in cases of: Application: Contraindications: Adverse reactions: Interactions with other remedies: Side effects: Precautions:

Unless otherwise prescribed: 3-4 x daily 5 drops. None known. None known.

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

302

Advice: How supplied:

The preparation contains 20 % (v/v) alcohol (ethanol). The following dosage forms are available: 10 ml and 30 ml dropper bottle 4X, 2 ml ampule 10 and 50 4X.

303

Selenokehl 4X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Sodium selenite 4X 1 ampule of 2 ml contains: Medically active substance: 0.16 ml Sodium selenite 4X aqueous dilut. Other constituents: isotonic sodium chloride solution. Selenium is an essential trace element. In the human body it is chiefly connected with the enzyme glutathione peroxidase which is a constituent of the antioxidative protective system of the cell. In test models it has been proven that the selenium-containing glutathione peroxidase is one of the strongest, most effective enzymes of the body for absorbing radicals. Among other benefits, it lowers the rate of peroxidation of lipids and thereby protects the cellular membrane from damages. Deficiency in selenium increases the toxicity of heavy metals such as mercury, lead and cadmium, and also it potentizes weakness of the liver that is due to oxidative and chemical influences. The significance of selenium as an antioxidant, also its anti-carcinogenic and anti-mutagenic properties, have been well researched. It has been proven in numerous tests that a continuing intake of selenium can inhibit chemically and virally induced tumorous developments. This is valid especially for tumorous systems such as skin, liver, intestinal and breast cancer. Selenium deficiency due to malnutrition and malabsorption, for amalgam detoxification.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 2 ml to be injected either intramuscularly, subcutaneously or intravenously, 1 x daily. None known. None known.

Contraindications: Adverse reactions: Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children.

304

Duration of treatment: How supplied:

Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml and 30 ml dropper bottle 4X, 2 ml ampule 10 and 50 4X.

305

Silvaysan
Capsules
For oral intake

Active ingredient: Composition:

Dry extract from Silybum marianum 1 capsule contains: Medically active substance: 136 - 160 mg dry extract from Silybum marianum (50-70:1) equivalent to 110 mg Silymarin, taken into account for Silibinin (extractive substance: acetone). Standardisation material: dextrose 0 to 24 mg. Other constituents: highly dispersed silica, dextrose, lactose 1 H2O, magnesium stearate, gelatin, purified water. Silymarin has an antogonistic effect on several types of liver disorders: fungal poisons phalloidin and -amanitin, lanthanum, carbon tetrachloride, galactosamine, thioacetamide as well as the hepatotoxic of coldblooded animals virus FV3. Silymarins therapeutic effects are based on two points of application or modes of action: Silymarin changes the structure of the outer cell membrane of the hepatocytes in such a way that hepatotoxins cannot enter into the cell. Silymarin stimulates the activity of the nucleolar polymerase A, resulting in an increased ribosomal protein synthesis, thus stimulating the regenerative power of the liver and the neogenesis of hepatocytes. Supporting treatment of chronic inflammatory liver diseases and cirrhosis of the liver as well as toxic liver damage. Unless otherwise prescribed: adults and adolescents from 12 years onwards 3 capsules taken daily with some liquid. None known. None known. Because of specific organic components of Silvaysan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

Indication:

Application:

Contraindications: Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. Sometimes a slight sporadic cathartic effect may be observed. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

306

Advice:

The drug therapy does not replace the avoidance of the hepatotoxic causes (e.g. alcohol). In case of icterus (light- to dark-yellow coloured skin, yellow coloured sclera) professional medical advice should be sought immediately. Silvaysan is not suitable for the treatment of acute intoxication. The following dosage forms are available: 20 and 100 capsules.

How supplied:

307

Stolonikehl 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Penicillium stoloniferum extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Penicillium stoloniferum 6X dil. Other constituents: purified water.

Characteristics:

Penicillium stoloniferum, an ubiquitous mold fungus was already in the 1950s for possessing anti-viral activities. Systematic studies have shown prophylactic properties against artificial viral infections where a strong interferon induction as mechanism of action was discussed. In the 1960s, the isolation of the virucidal substance was achieved and was named Statolon. A remedy was then developed prepared from the mycelia of the fungus analogously to the already known mold fungus preparations.
Intercostal neuralgia.

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops before a meal. For rubbing in: 1 x daily 5-10 drops at the location of the disease or into the bend of the elbow. In case of simultaneous treatment with injections, rub in 2 x weekly 5-10 drops on injection-free days. In cases of known hypersensitivity to Penicillium stoloniferum, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Stolonikehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage form is available: 10 ml dropper bottle 6X.

Duration of treatment: How supplied:

308

Strophanthus 4X Sanum
Drops
Liquid dilution for oral intake

Active ingredient: Composition:

Strophanthus gratus extract 4X 1 ml liquid dilution contains: Medically active substance: 1 ml Strophanthus gratus 4X dil. Other constituents: purified water, ethanol. Strophanthin, also known as Ouabain, was used by the african natives as arrow poison for a long time. It is produced from a milk-secreting climbing plant, but it is also an endogenous hormone which is produced in the adrenal gland and is involved in the regulation of the balance of salt and water. An isomer of g-Strophanthin is contained in human hypophysis which de lays the sodium pump. Therefore, g-Strophanthin is an endogenic substance. Because of his influence, the myocardial work can be relieved fundamentally. The administration of g-Strophanthin can absorb a weakness of the adrenal gland which possibly occur with increasing age and thereby supports the weak senile heart. Cardiac weakness, increasing blood volume, hypertension, sodium burden, nervous heart by reason of smoking, arteriosclerosis, cardiac decompensation; anticipatory anxiety; bleeding and profuse blockage of the uterine region Unless otherwise prescribed: In case of acute conditions 5 drops every half to one hour (max. 12 times per day), for chronic forms 1-3 x daily 5 drops. None known. None known. Because of specific organic components of Strophanthus 4X Sanum, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications: Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

309

Advice: How supplied:

The preparation contains 51 % (v/v) alcohol (ethanol). The following dosage forms are available: 10 ml, 30ml, 100 ml dropper bottle 4X, 80 tablets 4X.

310

Strophanthus 4X Sanum
Tablets

Active ingredient: Composition:

Strophanthus gratus extract 4X 1 tablet contains: Medically active substance: 250 mg Strophanthus gratus 4X trit. Other constituents: lactose, potato starch, magnesium stearate. Strophanthin, also known as Ouabain, was used by the african natives as arrow poison for a long time. It is produced from a milk-secreting climbing plant, but it is also an endogenous hormone which is produced in the adrenal gland and is involved in the regulation of the balance of salt and water. An isomer of g-Strophanthin is contained in human hypophysis which delays the sodium pump. Therefore, g-Strophanthin is an endogenic substance. Because of his influence, the myocardial work can be relieved fundamentally. The administration of g-Strophanthin can absorb a weakness of the adrenal gland which possibly occur with increasing age and thereby supports the weak senile heart. Cardiac weakness, increasing blood volume, hypertension, sodium burden, nervous heart by reason of smoking, arteriosclerosis, cardiac decompensation; anticipatory anxiety; bleeding and profuse blockage of the uterine region Unless otherwise prescribed: In case of acute conditions: 1 tablet every half to one hour (max. 12 times per day), for chronic forms: 1-3 x daily 1 tablet. None known. None known. Because of specific organic components of Strophanthus 4X Sanum, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications: Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml, 30ml, 100 ml dropper bottle 4X, 80 tablets 4X.

Duration of treatment: How supplied:

311

Thymokehl 6X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Thymus glands extract (calf) 6X 1 ampule of 2 ml contains: Medically active substance: 2 ml thymus glands extract (calf) 6X aqueous dilut. Other constituents: isotonic sodium chloride solution. Extracts from organs act positively on the entire cellular metabolism. In cellular therapy, research has shown that materials resorbed from organ extracts promote the cellular repair processes on the DNA. They act as a stimulant where damaged cells need to be regenerated and supplemented where degenerated cells break down. The thymus extract in Thymokehl shows an identical physiologic activity and, with little differentiation in its molecular structure to that of the human organ. The promotion of cellular respiration by the thymus extract has been proven in various animal test models. Of the special thymus factors, the Thymosin 1 peptide has been isolated. This stimulates the premature T-lymphocytes into maturing, thus increasing their numbers. Disorders in growth and development, for all degenerative processes in the lumbar vertebral column area.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 2 to 4 ml to be injected either intramuscularly or subcutaneously, 2-3 x weekly. In cases of known hypersensitivity to animal protein, especially calf protein, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Thymokehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

312

Advice:

The concurrent application of Rebas, also an immunologically active substance, intensifies the action of Thymokehl. In addition to Thymokehl induced T-lymphocyte proliferation, Rebas encourages the formation of humoral antibodies by stimulating the T-helper cells. The following dosage forms are available: 2 ml ampule 10 and 50 6X, 10 suppositories 6X, 20 capsules 6X.

How supplied:

313

Thymokehl 6X
Capsules
For oral intake

Active ingredient: Composition:

Thymus glands extract (calf) 6X 1 capsule contains: Medically active substance: 330 mg thymus glands extract (calf) 6X trit. Other constituents: lactose, hypromellosis (capsule shell). Extracts from organs act positively on the entire cellular metabolism. In cellular therapy, research has shown that materials resorbed from organ extracts promote the cellular repair processes on the DNA. They act as a stimulant where damaged cells need to be regenerated and supplemented where degenerated cells break down. The thymus extract in Thymokehl shows an identical physiologic activity and, with little differentiation in its molecular structure to that of the human organ. The promotion of cellular respiration by the thymus extract has been proven in various animal test models. Of the special thymus factors, the Thymosin 1 peptide has been isolated. This stimulates the premature T-lymphocytes into maturing, thus increasing their numbers. Disorders in growth and development, for all degenerative processes in the lumbar vertebral column area.

Characteristics:

According to experience, to be administered in cases of: Application: Contraindications:

Unless otherwise prescribed: 1-3 capsules daily before a meal. In cases of known hypersensitivity to animal protein, especially calf protein, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Thymokehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

314

Advice:

The concurrent application of Rebas, also an immunologically active substance, intensifies the action of Thymokehl. In addition to Thymokehl induced T-lymphocyte proliferation, Rebas encourages the formation of humoral antibodies by stimulating the T-helper cells. The following dosage forms are available: 2 ml ampule 10 and 50 6X, 10 suppositories 6X, 20 capsules 6X.

How supplied:

315

Thymokehl 6X
Suppositories

Active ingredient: Composition:

Thymus glands extract (calf) 6X 1 suppository contains: Medically active substance: 0.2 g thymus glands extract (calf) 6X trit. Other constituents: hard fat, lactose. Extracts from organs act positively on the entire cellular metabolism. In cellular therapy, research has shown that materials resorbed from organ extracts promote the cellular repair processes on the DNA. They act as a stimulant where damaged cells need to be regenerated and supplemented where degenerated cells break down. The thymus extract in Thymokehl shows an identical physiologic activity and, with little differentiation in its molecular structure to that of the human organ. The promotion of cellular respiration by the thymus extract has been proven in various animal test models. Of the special thymus factors, the Thymosin 1 peptide has been isolated. This stimulates the premature T-lymphocytes into maturing, thus increasing their numbers. Disorders in growth and development, for all degenerative processes in the lumbar vertebral column area.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 x daily 1 suppository to be inserted rectally at bedtime. In cases of known hypersensitivity to animal protein, especially calf protein, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Thymokehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

316

Advice:

The concurrent application of Rebas, also an immunologically active substance, intensifies the action of Thymokehl. In addition to Thymokehl induced T-lymphocyte proliferation, Rebas encourages the formation of humoral antibodies by stimulating the T-helper cells. The following dosage forms are available: 2 ml ampule 10 and 50 6X, 10 suppositories 6X, 20 capsules 6X.

How supplied:

317

Usneabasan 1X
Drops
Liquid dilution for oral intake

Active ingredient: Composition:

Usnea barbata extract 1X 1 ml liquid dilution contains: Medically active substance: 1 ml Usnea barbata 1X dil. Other constituents: purified water, ethanol. Beardmoss (Usnea barbata) is a plant from which Usneabasan is produced. Its main scope of application lies in the area of the head. Usnea barbata has long been used in homeopathy for congestive headaches. It is also administered for redness of the face, a knocking or bursting sensation in the temple region, in the eyes and the back of the head. Congestive headaches, sunstroke, elimination of heavy metals.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For oral intake: In case of acute conditions: 5 drops every half to one hour. For chronic forms: 1-3 x daily 5 drops. None known. None known. Because of specific organic components of Usneabasan, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications: Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The preparation contains 70 % (v/v) alcohol (ethanol). The following dosage forms are available: 30 ml dropper bottle 1X.

Duration of treatment: Advice: How supplied:

318

Ustilakehl 5X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Ustilago zeae extract 5X 1 ml liquid dilution contains: Medically active substance: 1 ml Ustilago zeae e sporibus rec. 5X dil. Other constituents: purified water.

Characteristics:

Ustilago zeae, the corn-smut is a parasitary fungus that attacks all parts of the maize plant and forms bump-like distensions filled with spore powder. The fungus has a very complicated developmental cycle with different mycelia and spore stages and represents the rare sample of a yeast forming basidiomycetes. From the latter growth form the preparation Ustilakehl which is manufactured, analogous to the procedure developed by Prof. Enderlein. As the maize plant itself, the first medicinal use of the drug came from America. It was predominantly used in folk medicine by the AfroAmerican population. The ergotamine-like effect of the corn-smut in the uterus causes its main effect.
Uterine haemorrhage, membranous dysmenorrhoea, menopausal syndrome, menorrhagia, metrorrhagia, headache caused by menstruation, migraine. Unless otherwise prescribed: For oral intake: 1 x daily 5-10 drops before a meal. For rubbing in: 1 x daily 5-10 drops at the location of the disease or into the bend of the elbow. In case of simultaneous treatment with injections, rub in 2 x weekly 5-10 drops on injection-free days. In cases of known hypersensitivity to Ustilago zeae, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Ustilakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

319

Advice: How supplied:

Bottle must be used within 2 months. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 5X.

320

Ustilakehl 5X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Ustilago zeae extract 5X 1 ampule of 1 ml contains: Medically active substance: 1 ml Ustilago zeae e sporibus rec. 5X aqueous dilut. Other constituents: isotonic sodium chloride solution.

Characteristics:

Ustilago zeae, the corn-smut is a parasitary fungus that attacks all parts of the maize plant and forms bump-like distensions filled with spore powder. The fungus has a very complicated developmental cycle with different mycelia and spore stages and represents the rare sample of a yeast forming basidiomycetes. From the latter growth form the preparation Ustilakehl which is manufactured, analogous to the procedure developed by Prof. Enderlein. As the maize plant itself, the first medicinal use of the drug came from America. It was predominantly used in folk medicine by the AfroAmerican population. The ergotamine-like effect of the corn-smut in the uterus causes its main effect.
Uterine haemorrhage, membranous dysmenorrhoea, menopausal syndrome, menorrhagia, metrorrhagia, headache caused by menstruation, migraine. Unless otherwise prescribed: 1 ampule of 1 ml to be injected subcutaneously 2 x weekly. In cases of known hypersensitivity to Ustilago zeae, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Ustilakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 5X.

Duration of treatment: How supplied:

321

Ustilakehl 5X
Suppositories

Active ingredient: Composition:

Ustilago zeae extract 5X 1 suppository contains: Medically active substance: 0.2 g Ustilago zeae e sporibus rec. 5X trit. Other constituents: hard fat, lactose.

Characteristics:

Ustilago zeae, the corn-smut is a parasitary fungus that attacks all parts of the maize plant and forms bump-like distensions filled with spore powder. The fungus has a very complicated developmental cycle with different mycelia and spore stages and represents the rare sample of a yeast forming basidiomycetes. From the latter growth form the preparation Ustilakehl which is manufactured, analogous to the procedure developed by Prof. Enderlein. As the maize plant itself, the first medicinal use of the drug came from America. It was predominantly used in folk medicine by the AfroAmerican population. The ergotamine-like effect of the corn-smut in the uterus causes its main effect.
Uterine haemorrhage, membranous dysmenorrhoea, menopausal syndrome, menorrhagia, metrorrhagia, headache caused by menstruation, migraine. Unless otherwise prescribed: 1 x daily, insert 1 suppository rectally at bedtime. In cases of known hypersensitivity to Ustilago zeae, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Ustilakehl, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 10 ml dropper bottle 5X, 1 ml ampule 10 and 50 5X, 10 suppositories 5X.

Duration of treatment: How supplied:

322

U t i l i n 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Bacillus subtilis extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Bacillus subtilis 6X dil. Other constituents: purified water. Utilin, not acid-proof, produced from Bacillus subtilis, a non-pathogenic spore-forming bacillus is a mild irritative therapeutic (non-specific immunization). It does not cause any significant rise in temperature or general reactions. Utilin has proven itself over years for the activation of endogenic defense functions and especially for rheumatic diseases. In immunological test models, a significant rise in phagocytic activity of the granulocytes has been established. A strong rise in T-lymphocyte proliferation also confirms Utilin as a potent immune modulator. All sub-acute and chronic inflammations in respiratory, intestinal and urogenital tract, for immune modulation, especially rheumatic diseases and Basedow. Unless otherwise prescribed: For oral intake: 1-3 x daily 2-5 drops before a meal. For rubbing in: 2-3 x weekly 5-10 drops at the location of the disease or into the bend of the elbow. In cases of known hypersensitivity to Bacillus subtilis, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Utilin, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

323

Advice:

In isopathic therapy, Utilin is used as an irritative agent for unspecific immunostimulaton. The alternating administration of Utilin and Recarcin has proved to be successful. A noticeable stimulus threshold is also attributed to the good effects of Utilin. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

How supplied:

324

U t i l i n 4X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Bacillus subtilis extract 4X 1 ampule of 1 ml contains: Medically active substance: 1 ml Bacillus subtilis 4X aqueous dilut. Other constituents: isotonic sodium chloride solution. Utilin, not acid-proof, produced from Bacillus subtilis, a non-pathogenic spore-forming bacillus is a mild irritative therapeutic (non-specific immunization). It does not cause any significant rise in temperature or general reactions. Utilin has proven itself over years for the activation of endogenic defense functions and especially for rheumatic diseases. In immunological test models, a significant rise in phagocytic activity of the granulocytes has been established. A strong rise in T-lymphocyte proliferation also confirms Utilin as a potent immune modulator. All sub-acute and chronic inflammations in respiratory, intestinal and urogenital tract, for immune modulation, especially rheumatic diseases and Basedow. Unless otherwise prescribed: 1 ampule of 1 ml to be injected deep intramuscularly - regular intragluteally - while the patient is lying down, every two weeks. Normally the treatment is started with the administration of capsules 6X or 4X or with injection 6X. In case of absent or weak reactions the dosage may be gradually raised by shorter intervals - 2 ampules weekly at the most. In case of strong reactions, injections have to be discontinued; the treatment can be continued with the dosage form capsules. As a general advice the dosage has to be chosen adequately, so that strong general reactions do not occur and that local reactions are confined to the site of injections. Fever, conditions of weakness. In cases of known hypersensitivity to Bacillus subtilis, as a precaution, this preparation should not be administered. None known. Generally well tolerated. Occasionally local reactions like rubefaction, swelling or painfulness may be observed, normally vanishing without treatment. These effects are not to be seen as adverse reactions, but rather as an expression of effectiveness. In the first 2 or 3 days after the injection sometimes conditions of weakness, fortified expectoration, slight painfulness of the region or subfebrile temperatures may occur. Strong general reactions are always a sign of overdosage or of incorrect injection technique. In this case the treatment can be continued orally with Utilin capsules 6X or 4X.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

325

Interactions with other remedies:

None known. An interval of four weeks should be kept to the administration of vaccinations. In cases of simultaneous treatment with immunosuppressive remedies, the effectiveness of Utilin may be influenced. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. In isopathic therapy, Utilin is used as an irritative agent for unspecific immunostimulation. The alternating administration of Utilin and Recarcin has proved to be successful. A noticeable stimulus threshold is also attributed to the good effects of Utilin. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

Side effects: Precautions:

Duration of treatment: Advice:

How supplied:

326

U t i l i n 6X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Bacillus subtilis extract 6X 1 ampule of 1 ml contains: Medically active substance: 1 ml Bacillus subtilis 6X aqueous dilut. Other constituents: isotonic sodium chloride solution. Utilin, not acid-proof, produced from Bacillus subtilis, a non-pathogenic spore-forming bacillus is a mild irritative therapeutic (non-specific immunization). It does not cause any significant rise in temperature or general reactions. Utilin has proven itself over years for the activation of endogenic defense functions and especially for rheumatic diseases. In immunological test models, a significant rise in phagocytic activity of the granulocytes has been established. A strong rise in T-lymphocyte proliferation also confirms Utilin as a potent immune modulator. All sub-acute and chronic inflammations in respiratory, intestinal and urogenital tract, for immune modulation, especially rheumatic diseases and Basedow. Unless otherwise prescribed: 1 ampule of 1 ml to be injected deep intramuscularly - regular intragluteally - while the patient is lying down, every two weeks. Normally the treatment is started with the administration of capsules 6X or 4X. In case of absent or weak reactions the dosage may be gradually raised by shorter intervals - 2 ampules weekly at the most - and/ or by the injection of strength 4X. In case of strong reactions, injections have to be discontinued; the treatment can be continued with the dosage form capsules. As a general advice the dosage has to be chosen adequately, so that strong general reactions do not occur and that local reactions are confined to the site of injections. Fever, conditions of weakness. In cases of known hypersensitivity to Bacillus subtilis, as a precaution, this preparation should not be administered. None known. Generally well tolerated. Occasionally local reactions like rubefaction, swelling or painfulness may be observed, normally vanishing without treatment. These effects are not to be seen as adverse reactions, but rather as an expression of effectiveness. In the first 2 or 3 days after the injection sometimes conditions of weakness, fortified expectoration, slight painfulness of the region or subfebrile temperatures may occur. Strong general reactions are always a sign of overdosage or of incorrect injection technique. In this case the treatment can be continued orally with Utilin capsules 6X or 4X.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

327

Interactions with other remedies:

None known. An interval of four weeks should be kept to the administration of vaccinations. In cases of simultaneous treatment with immunosuppressive remedies, the effectiveness of Utilin may be influenced. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. In isopathic therapy, Utilin is used as an irritative agent for unspecific immunostimulation. The alternating administration of Utilin and Recarcin has proved to be successful. A noticeable stimulus threshold is also attributed to the good effects of Utilin. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

Side effects: Precautions:

Duration of treatment: Advice:

How supplied:

328

U t i l i n 4X
Capsules
For oral intake

Active ingredient: Composition:

Bacillus subtilis extract 4X 1 capsule contains: Medically active substance: 330 mg Bacillus subtilis 4X trit. Other constituents: lactose, hypromellosis (capsule shell). Utilin, not acid-proof, produced from Bacillus subtilis, a non-pathogenic spore-forming bacillus is a mild irritative therapeutic (non-specific immunization). It does not cause any significant rise in temperature or general reactions. Utilin has proven itself over years for the activation of endogenic defense functions and especially for rheumatic diseases. In immunological test models, a significant rise in phagocytic activity of the granulocytes has been established. A strong rise in T-lymphocyte proliferation also confirms Utilin as a potent immune modulator. All sub-acute and chronic inflammations in respiratory, intestinal and urogenital tract, for immune modulation, especially rheumatic diseases and Basedow. Unless otherwise prescribed: 1-2x weekly 1 capsule at bedtime, taken with some liquid. In cases of known hypersensitivity to Bacillus subtilis, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Utilin, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

329

Advice:

In isopathic therapy, Utilin is used as an irritative agent for unspecific immunostimulation. The alternating administration of Utilin and Recarcin has proved to be successful. A noticeable stimulus threshold is also attributed to the good effects of Utilin. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

How supplied:

330

U t i l i n 6X
Capsules
For oral intake

Active ingredient: Composition:

Bacillus subtilis extract 6X 1 capsule contains: Medically active substance: 330 mg Bacillus subtilis 6X trit. Other constituents: lactose, hypromellosis (capsule shell). Utilin, not acid-proof, produced from Bacillus subtilis, a non-pathogenic spore-forming bacillus is a mild irritative therapeutic (non-specific immunization). It does not cause any significant rise in temperature or general reactions. Utilin has proven itself over years for the activation of endogenic defense functions and especially for rheumatic diseases. In immunological test models, a significant rise in phagocytic activity of the granulocytes has been established. A strong rise in T-lymphocyte proliferation also confirms Utilin as a potent immune modulator. All sub-acute and chronic inflammations in respiratory, intestinal and urogenital tract, for immune modulation, especially rheumatic diseases and Basedow. Unless otherwise prescribed: 1-2x weekly 1 capsule at bedtime, taken with some liquid. In cases of known hypersensitivity to Bacillus subtilis, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Utilin, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

331

Advice:

In isopathic therapy, Utilin is used as an irritative agent for unspecific immunostimulation. The alternating administration of Utilin and Recarcin has proved to be successful. A noticeable stimulus threshold is also attributed to the good effects of Utilin. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

How supplied:

332

U t i l i n 6X
Suppositories

Active ingredient: Composition:

Bacillus subtilis extract 6X 1 suppository contains: Medically active substance: 0.2 g Bacillus subtilis 6X trit. Other constituents: hard fat, lactose. Utilin, not acid-proof, produced from Bacillus subtilis, a non-pathogenic spore-forming bacillus is a mild irritative therapeutic (non-specific immunization). It does not cause any significant rise in temperature or general reactions. Utilin has proven itself over years for the activation of endogenic defense functions and especially for rheumatic diseases. In immunological test models, a significant rise in phagocytic activity of the granulocytes has been established. A strong rise in T-lymphocyte proliferation also confirms Utilin as a potent immune modulator. All sub-acute and chronic inflammations in respiratory, intestinal and urogenital tract, for immune modulation, especially rheumatic diseases and Basedow. Unless otherwise prescribed: 1-3 x weekly 1 suppository, inserted into the rectum at bedtime. In cases of known hypersensitivity to Bacillus subtilis, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Utilin, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Characteristics:

According to experience, to be administered in cases of: Application:

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional.

Duration of treatment:

333

Advice:

In isopathic therapy, Utilin is used as an irritative agent for unspecific immunostimulation. The alternating administration of Utilin and Recarcin has proved to be successful. A noticeable stimulus threshold is also attributed to the good effects of Utilin. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

How supplied:

334

U t i l i n S 6X
Drops
Liquid dilution for oral intake, rubbing in

Active ingredient: Composition:

Mycobacterium phlei extract 6X 1 ml liquid dilution contains: Medically active substance: 1 ml Mycobacterium phlei 6X dil. Other constituents: purified water. Immunologic test models have shown that Utilin S stimulates the immune system in a specific and unspecific way e.g. a substantial rise in phagocytic activity of granulocytes was discovered. Furthermore a stimulation of the T-lymphocyte population for increased release of lymphokines is produced. Its tumor blocking effect results from the induction of interferon which raises the activity of natural killer cells and the toxicity of activated macrophages against tumor cells. The specific isopathic effect of Utilin S acts directly on all tubercular and paratubercular diseases. All chronic diseases of lung, chronic feverish diseases with night sweats and weakness, for immune modulation.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: For oral intake: 1-3 x daily 2-5 drops before a meal. For rubbing in: 2-3 x weekly 5-10 drops at the location of the disease or into the bend of the elbow. In cases of known hypersensitivity to Mycobacterium phlei, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Utilin S, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

Duration of treatment: How supplied:

335

U t i l i n S 4X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Mycobacterium phlei extract 4X 1 ampule of 1 ml contains: Medically active substance: 1 ml Mycobacterium phlei 4X aqueous dilut. Other constituents: isotonic sodium chloride solution. Immunologic test models have shown that Utilin S stimulates the immune system in a specific and unspecific way e.g. a substantial rise in phagocytic activity of granulocytes was discovered. Furthermore a stimulation of the T-lymphocyte population for increased release of lymphokines is produced. Its tumor blocking effect results from the induction of interferon which raises the activity of natural killer cells and the toxicity of activated macrophages against tumor cells. The specific isopathic effect of Utilin S acts directly on all tubercular and paratubercular diseases. All chronic diseases of lung, chronic feverish diseases with night sweats and weakness, for immune modulation.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 1 ml to be injected deep intramuscularly - regular intragluteally - while the patient is lying down, every two weeks. Normally the treatment is started with the administration of capsules 6X or 4X or with injection 6X. In case of absent or weak reactions the dosage may be gradually raised by shorter intervals - 2 ampules weekly at the most. In case of strong reactions, injections have to be discontinued; the treatment can be continued with the dosage form capsules. As a general advice the dosage has to be chosen adequately, so that strong general reactions do not occur and that local reactions are confined to the site of injections. Fever, conditions of weakness. In cases of known hypersensitivity to Mycobacterium phlei, as a precaution, this preparation should not be administered. None known. Generally well tolerated. Occasionally local reactions like rubefaction, swelling or painfulness may be observed, normally vanishing without treatment. These effects are not to be seen as adverse reactions, but rather as an expression of effectiveness. In the first 2 or 3 days after the injection sometimes conditions of weakness, fortified expectoration, slight painfulness of the region or subfebrile temperatures may occur. Strong general reactions are always a sign of overdosage or of incorrect injection technique. In this case the treatment can be continued orally with Utilin S capsules 6X or 4X.

Contraindications:

Adverse reactions:

336

Interactions t with other remedies:

None known. An interval of four weeks should be kept to the administrai o n of vaccinations. In cases of simultaneous treatment with immunosuppressive remedies, the effectiveness of Utilin S may be influenced. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. Shake well before use. Utilin S is used in isopathic therapy as an irritative agent for all subacute to chronic relapsing infections, especially to the area of the head. Increased toxin elimination is important before administering Utilin S. A noticeable stimulus threshold is also attributed to the good effect of Utilin S is achieved. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

Side effects: Precautions:

Duration of treatment: Advice:

How supplied:

337

U t i l i n S 6X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Mycobacterium phlei extract 6X 1 ampule of 1 ml contains: Medically active substance: 1 ml Mycobacterium phlei 6X aqueous dilut. Other constituents: isotonic sodium chloride solution. Immunologic test models have shown that Utilin S stimulates the immune system in a specific and unspecific way e.g. a substantial rise in phagocytic activity of granulocytes was discovered. Furthermore a stimulation of the T-lymphocyte population for increased release of lymphokines is produced. Its tumor blocking effect results from the induction of interferon which raises the activity of natural killer cells and the toxicity of activated macrophages against tumor cells. The specific isopathic effect of Utilin S acts directly on all tubercular and paratubercular diseases. All chronic diseases of lung, chronic feverish diseases with night sweats and weakness, for immune modulation.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 ampule of 1 ml to be injected deep intramuscularly - regular intragluteally - while the patient is lying down, every two weeks. Normally the treatment is started with the administration of capsules 6X or 4X. In case of absent or weak reactions the dosage may be gradually raised by shorter intervals - 2 ampules weekly at the most - and/ or by the injection of strength 4X. In case of strong reactions, injections have to be discontinued; the treatment can be continued with the dosage form capsules. As general advice the dosage has to be chosen adequately, so that strong general reactions do not occur and that local reactions are confined to the site of injections. Fever, conditions of weakness. In cases of known hypersensitivity to Mycobacterium phlei, as a precaution, this preparation should not be administered. None known. Generally well tolerated. Occasionally local reactions like rubefaction, swelling or painfulness may be observed, normally vanishing without treatment. These effects are not to be seen as adverse reactions, but rather as an expression of effectiveness. In the first 2 or 3 days after the injection sometimes conditions of weakness, fortified expectoration, slight painfulness of the region or subfebrile temperatures may occur. Strong general reactions are always a sign of overdosage or of incorrect injection technique. In this case the treatment can be continued orally with Utilin S capsules 6X or 4X.

Contraindications:

Adverse reactions:

338

Interactions t with other remedies:

None known. An interval of four weeks should be kept to the administrai o n of vaccinations. In cases of simultaneous treatment with immunosuppressive remedies, the effectiveness of Utilin S may be influenced. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. Shake well before use. Utilin S is used in isopathic therapy as an irritative agent for all subacute to chronic relapsing infections, especially to the area of the head. Increased toxin elimination is important before administering Utilin S. A noticeable stimulus threshold is also attributed to the good effect of Utilin S. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

Side effects: Precautions:

Duration of treatment: Advice:

How supplied:

339

U t i l i n S 4X
Capsules
For oral intake

Active ingredient: Composition:

Mycobacterium phlei extract 4X 1 capsule contains: Medically active substance: 330 mg Mycobacterium phlei 4X trit. Other constituents: lactose, hypromellosis (capsule shell). Immunologic test models have shown that Utilin S stimulates the immune system in a specific and unspecific way e.g. a substantial rise in phagocytic activity of granulocytes was discovered. Furthermore a stimulation of the T-lymphocyte population for increased release of lymphokines is produced. Its tumor blocking effect results from the induction of interferon which raises the activity of natural killer cells and the toxicity of activated macrophages against tumor cells. The specific isopathic effect of Utilin S acts directly on all tubercular and paratubercular diseases. All chronic diseases of lung, chronic feverish diseases with night sweats and weakness, for immune modulation.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1-2x weekly 1 capsule at bedtime, taken with some liquid. In cases of known hypersensitivity to Mycobacterium phlei, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Utilin S, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. Utilin S is used in isopathic therapy as an irritative agent for all subacute to chronic relapsing infections, especially to the area of the head. A noticeable stimulus threshold is also attributed to the good effect of Utilin S. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

Duration of treatment: Advice:

How supplied:

340

U t i l i n S 6X
Capsules
For oral intake

Active ingredient: Composition:

Mycobacterium phlei extract 6X 1 capsule contains: Medically active substance: 330 mg Mycobacterium phlei 6X trit. Other constituents: lactose, hypromellosis (capsule shell). Immunologic test models have shown that Utilin S stimulates the immune system in a specific and unspecific way e.g. a substantial rise in phagocytic activity of granulocytes was discovered. Furthermore a stimulation of the T-lymphocyte population for increased release of lymphokines is produced. Its tumor blocking effect results from the induction of interferon which raises the activity of natural killer cells and the toxicity of activated macrophages against tumor cells. The specific isopathic effect of Utilin S acts directly on all tubercular and paratubercular diseases. All chronic diseases of lung, chronic feverish diseases with night sweats and weakness, for immune modulation.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1-2x weekly 1 capsule at bedtime, taken with some liquid. In cases of known hypersensitivity to Mycobacterium phlei, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Utilin S, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. Utilin S is used in isopathic therapy as an irritative agent for all subacute to chronic relapsing infections, especially to the area of the head. A noticeable stimulus threshold is also attributed to the good effect of Utilin S. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

Duration of treatment: Advice:

How supplied:

341

U t i l i n S 6X
Suppositories

Active ingredient: Composition:

Mycobacterium phlei extract 6X 1 suppository contains: Medically active substance: 0.2 g Mycobacterium phlei 6X trit. Other constituents: hard fat, lactose. Immunologic test models have shown that Utilin S stimulates the immune system in a specific and unspecific way e.g. a substantial rise in phagocytic activity of granulocytes was discovered. Furthermore a stimulation of the T-lymphocyte population for increased release of lymphokines is produced. Its tumor blocking effect results from the induction of interferon which raises the activity of natural killer cells and the toxicity of activated macrophages against tumor cells. The specific isopathic effect of Utilin S acts directly on all tubercular and paratubercular diseases. All chronic diseases of lung, chronic feverish diseases with night sweats and weakness, for immune modulation.

Characteristics:

According to experience, to be administered in cases of: Application:

Unless otherwise prescribed: 1 - 3 x weekly 1 suppository, inserted into the rectum at bedtime. In cases of known hypersensitivity to Mycobacterium phlei, as a precaution, this preparation should not be administered. None known. Because of specific organic components of Utilin S, theoretically, hypersensitivity may occur. In this case, discontinue medication and treat symptomatically.

Contraindications:

Adverse reactions:

Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. Utilin S is used in isopathic therapy as an irritative agent for all subacute to chronic relapsing infections, especially to the area of the head. A noticeable stimulus threshold is also attributed to the good effect of Utilin S. The following dosage forms are available: 5 ml dropper bottle 6X, 1 ml ampule 10 and 50 4X, 6X, 10 suppositories 6X, 5 capsules 4X, 6X.

Duration of treatment: Advice:

How supplied:

342

Vitamin B Komplex Sanum N


Ampules
Liquid dilution for injection

Active ingredient:

Thiamine hydrochloride (vitamin B1), Pyridoxine hydrochloride (vitamin B6) 1 ampule of 2 ml contains: Medically active substances: 10 mg Thiamine hydrochloride (vitamin B1), 5 mg Pyridoxine hydrochloride (vitamin B6). Other constituents: Benzyl alcohol. Vitamin B1 (thiamine) in its active form, thiamine pyrophosphate (TPP), plays a crucial role in the carbohydrate metabolism. The daily requirement of vitamin B1 depends on the type of nutrition consumed. If one consumes mainly carbohydrates, then the requirement of vitamin B1 increases. A pure vitamin B1 deficiency causes reduced mental and physical power, lack of appetite and muscular atrophie, in particular to the lower extremities. Vitamin B6 is found in all living cells and its effective compound, pyridoxal-5phosphate, is an indispensable coenzyme in the amino acid metabolism. In cases of protein rich nutrition, the requirement of vitamin B6 is increased as well as during pregnancy and in cases of hyperthyroidism. A vitamin B6 deficiency can result in particular forms of anaemia as well as in skin diseases. Neuritis, neuralgia, trigeminal neuralgia, ischialgia, cervical syndrome, herpes zoster, radiculoneuritis because of degenerative spondylopathy. Vitamin B Komplex Sanum N has to be injected slowly intraveneously or intramuscularly. Unless otherwise prescribed: For initial treatment during the first days of therapy intramuscular injection daily with 1 ampule of 2 ml, after beginning of recovery 2-3 x weekly 1 ampule. In case of suspected vitamin B1 hypersensitivity Vitamin B Komplex Sanum N must not be used. None known. Vitamin B1 is broken down in sulphite containing infusion solutions. High dosages of vitamin B6 can weaken the effect of L-Dopa. In case of simultaneous use of isoniazid (INH), d-penicillamin and cycloserine the effectiveness of vitamin B6 can be lowered. In individual cases, hypersensitivity reactions with skin, urticaria and states of shock, particularly with allergy prone patients may appear. Hypersensitivity caused by benzyl alcohol rarely occurs.

Composition:

Characteristics:

Indications:

Application:

Contraindications:

Adverse reactions: Interactions with other remedies:

Side effects:

343

Precautions:

As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. Because Vitamin B Komplex Sanum N contains 20 mg benzyl alcohol as preservative, it must not be administered to new-born and undeveloped premature babies. 2 ml ampules 10 and 50.

Duration of treatment: Advice:

How supplied:

344

Vitamin E Sanum
Ampules
Liquid dilution for injection

Active ingredient: Composition:

RRR--tocopheryl acetate 1 ampule of 2 ml contains: Medically active substance: 150 mg RRR-tocopheryl acetate (=204 IU). Other constituents: -tocopherol, benzyl alcohol, ethyloleate, middle chained triglycerides. -tocopherol belongs to the group of E-vitamins (tocopherols) and has the highest biological activity of the tocopherols. The biochemical functions of vitamin E are extensively clarified. Vitamin E interferes in the intermediary metabolism, as well as acting as a radical catcher, saving polyunsaturated fatty acids of tissue and membrane lipids and other oxidation-sensitive substances (SH-groups of enzymes, vitamin A) in the organism against oxidative destruction. According to newer findings, vitamin E has an effect on the development of prostacyclin-thromboxane from which therapeutical administrations (e.g. arteriosclerosis) are derived. Deficiency situations can occur in combination with disturbances of fat digestion or fat resorption, e.g. with a pancreas insufficieny or obstruction of the bile duct. Therapy of vitamin E-deficiencies Injection intramuscular! Ignoring this, e.g. by intraveneous administration, dependent on the dosage to be applied, could cause an embolism through the oily part of the dilution and to a hemolysis through the emulgator. Intraveneous application must be avoided! Not suitable for intra-articular injection! The initial treatment should be carried out intraglutelly only with two ampules weekly. Normally four injections are given for initial therapy, thereafter continuing with oral medication of vitamin E. With disturbed fat resorption and in severe cases, the initial therapy should be continued for four weeks. None known. None known. Extreme high levels can interfere with the absorption of other fat-soluble vitamins. Sporadically anti-vitamin K-effects were reported with adults in anticoagulant treatment or vitamin K deficiency caused by malabsorption as well as with children with extremely high therapeutic serum levels of 1.1 g/l tocopherol, increasing the effect of vitamin K antagonists.

Characteristics:

Indications: Application:

Contraindications: Adverse reactions: Interactions with other remedies:

345

Side effects:

In rare cases temporary swelling or hardening of the injection area may appear. This can be avoided with careful injection. In order to avoid side effects, the injection should be administered slowly with relaxed muscles. Other severe side effects and hypervitaminosis are not known even with the administration of high doses over many years. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. Vitamin E Sanum contains benzyl alcohol. It must not be administered to new-born babies and especially not with those showing signs of prematurity. 2 ml ampules 10 and 50.

Precautions:

Duration of treatment: Advice:

How supplied:

346

Zinkokehl 3X
Drops
Liquid dilution for oral intake

Active ingredient: Composition:

Zinc gluconate 3X 1 ml liquid dilution contains: Medically active substance: 80 l Zinc gluconate 3X dil. Other constituents: purified water, ethanol. Zinc plays a significant role in the bodys mineral balance. Serious disorders and disease conditions can result with a prolonged or permanent lack of zinc, such as dwarfism, development deficiency, kidney damage, or skin infections. Weakness of the pancreas can be sucessfully treated with Zinkokehl when caused by a zinc deficiency. Zinc deficiencies can arise due to an unbalanced or poor diet. Disorders in the obligate, anaerobic intestinal flora, i.e. the absence of bacteroides and bifidus (still the cause of 80% of all primary and secondary intestinal disorders) are attributed to an excessive zinc deficiency. Zinkokehl is the first zinc remedy with zinc gluconate in homeopathic potentisation. For zinc deficiency conditions with: fractures, delayed bone growth, delayed healing of bones, coxarthrosis, pseudoarthrosis, rheumatic arthritis, psoriatic arthritis; skin diseases, such as eczema, acne, slow healing of wounds, burns, vegetative dysfunctions, dysbiosis and consecutive diseases such as cholecystitis, pancreatitis, diabetes mellitus; vein diseases such as thrombosis and ulcerations of the lower leg. Unless otherwise prescribed: In case of acute conditions: 5 drops every half to one hour. In case of chronic forms: 5 drops 1-3 x daily. None known. None known.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications: Adverse reactions: Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The preparation contains 20 % (v/v) alcohol (ethanol). The following dosage forms are available: 30 ml dropper bottle 3X, 2 ml ampule 10 and 50 4X.

Duration of treatment: Advice: How supplied:

347

Zinkokehl 4X
Ampules
Liquid dilution for injection

Active ingredient: Composition:

Zinc gluconate 4X 1 ampule of 2 ml contains: Medically active substance: 2 ml Zinc gluconate 4X aqueous dilut. Other constituents: isotonic sodium chloride solution. Zinc plays a significant role in the bodys mineral balance. Serious disorders and disease conditions can result with a prolonged or permanent lack of zinc, such as dwarfism, development deficiency, kidney damage, or skin infections. Weakness of the pancreas can be sucessfully treated with Zinkokehl when caused by a zinc deficiency. Zinc deficiencies can arise due to an unbalanced or poor diet. Disorders in the obligate, anaerobic intestinal flora, i.e. the absence of bacteroides and bifidus (still the cause of 80% of all primary and secondary intestinal disorders) are attributed to an excessive zinc deficiency. Zinkokehl is the first zinc remedy with zinc gluconate in homeopathic potentisation. For zinc deficiency conditions with: fractures, delayed bone growth, delayed healing of bones, coxarthrosis, pseudoarthrosis, rheumatic arthritis, psoriatic arthritis; skin diseases, such as eczema, acne, slow healing of wounds, burns, vegetative dysfunctions, dysbiosis and consecutive diseases such as cholecystitis, pancreatitis, diabetes mellitus; vein diseases such as thrombosis and ulcerations of the lower leg. Unless otherwise prescribed: 1 ampule of 2 ml to be injected either intramuscularly, subcutaneously, intracutaneously or intravenously, 1 x daily. None known. None known.

Characteristics:

According to experience, to be administered in cases of:

Application:

Contraindications: Adverse reactions: Interactions with other remedies: Side effects: Precautions:

None known. None known. As with all medications and due to the variations of clinical studies, professional medical advice should be sought prior to recommending this product to women during pregnancy or breastfeeding, as well as with children. Dependent on the advice of the physician or health care professional. The following dosage forms are available: 30 ml dropper bottle 3X, 2 ml ampule 10 and 50 4X.

Duration of treatment: How supplied:

348

Disease List
The following information is intended to serve as a quick reference guide for the practitioner and is not intended as a prescription outline. A thorough diagnosis and individual therapy plan is recommended in each case. It is assumed that through the participation of seminars specialising in the field of isopathic-homeopathy and pleomorphic research, that the naturopath gains a clearer insight of this form of therapy. An intensive introduction and training in SANUM therapy is possible through seminars and corresponding literature. Contact your distributor for information on future seminars.

Abscess, Mucokehl, Notakehl, Sanukehl Pseu, Sanukehl Staph Acidosis, Alkala N, Citrokehl, Sanuvis Acne, Latensin, Mucokehl, Nigersan, Notakehl, Pefrakehl, Polysan D, Sanukehl Myc, Sanukehl Staph, Utilin, Zinkokehl Acne vulgaris, Sanukehl Acne Acrodermatitis, Notakehl, Sankombi Acrodermatitis enterohepatica Fortakehl, Polysan Dx, Sanukehl Coli, Sanukehl Myc, Zinkokehl Actinomycosis, Mucokehl, Notakehl, Sanukehl Myc, Sanukehl Staph, Utilin S Addisons Disease, Mucokehl, Nigersan, Recarcin, Sankombi, Zinkokehl Adenoids, Mucokehl, Nigersan, Sankombi, Utilin Adnexitis, Fortakehl, Mucokehl, Nigersan, Notakehl, Pefrakehl, Sanukehl Myc, Sanukehl Strep, Utilin Agranulocytosis, Citrokehl, Formasan, Notakehl, Quentakehl, Sanukehl Pseu Alcohol Abuse, Alkala N, Citrokehl, Mucedokehl, Muscarsan, Vitamin B Komplex Sanum N Alkalinization, Alkala N, Citrokehl, Sanuvis

Allergic Asthma, see Allergy in general, Nigersan Allergy in general, Alkala N, Citrokehl, Exmykehl, Formasan, Fortakehl, Notakehl, Polysan K, Sanuvis, Utilin, Vitamin B Komplex Sanum N Allergic Diseases of the Gastrointestinal tract, see Allergy in general, Pefrakehl Allergic Rhinitis, Latensin, Nigersan, Notakehl, Sankombi, Utilin Alopecia (Baldness), Mucokehl, Pefrakehl, Pinikehl, Sanukehl Myc, Sanukehl Strep, Sankombi Alopecia areata, Mucokehl, Pinikehl, Sankombi Amenorrhea, Nigersan, Recarcin, Sanukehl Myc, Ustilakehl, Amoebiasis, Fortakehl, Okoubasan, Sanukehl Coli, Sanukehl Salm Anal Eczema, Exmykehl, Fortakehl, Pefrakehl, Sanukehl Cand Anal Fissures, Fortakehl, Mucokehl, Notakehl, Recarcin Anal Fistula, Fortakehl, Mucokehl, Nigersan, Notakehl, Pefrakehl, Recarcin, Sanukehl Pseu, Utilin Angina Pectoris, Leptospermusan, Mucokehl, Nigersan, Sanoryzae, Sanukehl Acne, Utilin Anginal Ulcers (Acute Sore Throat), Notakehl, Sankombi, Sanukehl Strep

347

Angioneurotic Edema, Fortakehl, Mucedokehl, Polysan Dx, Strophanthus Ankle Swelling, Leptucin, Mucokehl, Mucokehl Atox, Strophanthus Anthracosis, Formasan, Mucokehl, Polysan T, Recarcin, Sanukehl Staph Aphasia (see also Stroke), Mucokehl, Sankombi, Utilin Aphonia (see also Stroke), Sanukehl Myc Aphthous Ulcers, Fortakehl, Mucokehl, Notakehl, Pefrakehl, Quentakehl, Rebas, Recarcin, Sanukehl Cand, Sankombi Arrhythmia, Mucokehl, Sanukehl Myc, Sanukehl Strep, Strophanthus Arteriosclerosis, Citrokehl, Mucokehl, Nigersan, Polysan A, Sanumgerman, Sanuvis, Utilin Artery Disease in general, Leptucin, Leptospermusan, Mucedokehl, Mucokehl, Sanukehl Acne, Strophanthus Arthritis (Osteoarthritis), Arthrokehlan A, Latensin, Lipiscor, Mucokehl, Nigersan, Notakehl, Polysan D, Recarcin, Sankombi, Sanukehl Myc, Utilin, Utilin S Arthrosis, Fortakehl, Latensin, Lipiscor, Notakehl, Recarcin, Utilin S Asthma-Bronchitis, Fortakehl, Latensin, Mucokehl, Nigersan, Notakehl, Sanukehl Myc, Sanukehl Klebs, Sanukehl Pseu, Utilin, Utilin S, Vitamin B Komplex Sanum N Autonomic Nervous System Dysfunction, Latensin, Mucedokehl, Utilin, Vitamin B Komplex Sanum N, Zinkokehl Avitaminosis, Mapurit, Vitamin B Komplex Sanum N Balanitis, Albicansan, Pefrakehl Bed Wetting, Citrokehl, Latensin, Mucedokehl, Sankombi, Sanuvis, Utilin

Bladder Inflammation, see Cystitis Bleeding Tendencies, Calvakehl Blepharitis, Nigersan, Notakehl, Sanukehl Staph Blindness, Leptospermusan, Mucokehl, Utilin Bloating and Full Sensation, Alkala N Blood Poisoning, Notakehl, Polysan G, Quentakehl Breast Cancer, Alkala N, Exmykehl, Latensin, Mucokehl, Nigersan, Pefrakehl, Recarcin, Sanukehl Pseu, Sanuvis, Selenokehl, Utilin Bronchiectasis, Formasan, Notakehl, Sanukehl Klebs Bronchitis, Cerivikehl, Mucokehl, Notakehl, Quentakehl, Relivora Complex, Sankombi, Ruberkehl, Utilin, Utilin S Bruises, Mucokehl, Sanuvis Buccal Mucosal Inflammation, see Stomatitis Burns, Mucokehl, Notakehl, Sanukehl Pseu, Sankombi, Zinkokehl Candidiasis, Albicansan, Alkala N, Exmykehl, Fortakehl, Pefrakehl, Sanukehl Cand Carcinoma, Arthrokehlan U, Citrokehl, Exmykehl, Mucokehl, Nigersan, Notakehl, Pefrakehl, Polysan K, Polysan Om, Sankombi, Sanuvis, Sanukehl Pseu, Sanumgerman, Selenokehl, Utilin, Utilin S, Zinkokehl Cataract, Alkala N, Leptucin, Mucokehl (eye drops), Sanuvis, Silvaysan, Utilin S Cell Regeneration Therapy, Chrysocor, Citrokehl, Fortakehl, Leptospermusan, Mucokehl, Nigersan, Sanuvis Cephalgia, Alkala N, Citrokehl, Quentakehl, Sanukehl Myc, Usneabasan, Ustilakehl

348

Cervical Syndrome, Notakehl, Quentakehl, Usneabasan, Vitamin B Komplex Sanum N Chickenpox, Alkala N, Quentakehl, Sanuvis Childhood Diseases, Latensin, Notakehl, Pefrakehl, Sankombi, Utilin S Cholangitis, Citrokehl, Fortakehl, Latensin, Mucokehl, Notakehl, Pinikehl, Sanukehl Coli, Silvaysan, Utilin Cholecystitis, Albicansan, Fortakehl, Mucokehl, Notakehl, Pinikehl, Sanukehl Coli, Sanukehl Myc, Utilin, Usneabasan, Zinkokehl Chondrodystrophy, Citrokehl, Latensin, Mapurit, Mucokehl, Nigersan, Utilin, Utilin S Chronic Bronchitis, Cerivikehl, Fortakehl, Latensin, Quentakehl, Recarcin, Sanukehl Pseu, Utilin, Utilin S Chronic Dermatitis (Dermopathy), Citrokehl, Latensin, Mucokehl, Pefrakehl, Sanukehl Pseu, Sanuvis, Utilin, Chronic Dermatosis, Utilin, Zinkokehl Chronic Gastrointestinal Tract Inflammation, Fortakehl, Pefrakehl, Sanukehl Salm, Recarcin, Utilin Chronic Hepatitis, Pinikehl, Rebas, Sankombi, Silvaysan, Utilin Chronic Inflammation, Fortakehl, Latensin, Notakehl, Recarcin, Sanukehl Pseu, Utilin S Chronic Intestinal Diseases, Exmykehl, Fortakehl, Latensin, Sanukehl Brucel, Sanukehl Cand, Sanukehl Coli, Sanukehl Salm, Sanukehl Prot, Utilin Chronicity in general, Arthrokehlan U, Citrokehl, Fortakehl, Lipiscor, Mapurit, Pinikehl, Sankombi Chronic Mucosal Inflammation, Fortakehl, Latensin, Recarcin, Relivora Complex Chronic Pancreatitis, Alkala N, Citrokehl, Fortakehl, Pefrakehl, Pinikehl, Recarcin, Sanukehl Salm

Chronic Respiratory Tract Diseases, Citrokehl, Mucedokehl, Notakehl, Ruberkehl, Utilin, Utilin S Chronic Rheumatism, Arthrokehlan A, Citrokehl, Latensin, Notakehl, Sanukehl Pseu, Sanumgerman Chronic Urinary Tract Infection, Fomepikehl, Nigersan, Notakehl, Quentakehl, Sanukehl Coli, Sanukehl Myc Circulatory Problem of the Extremities, Leptospermusan, Leptucin, Mucedokehl, Mucokehl, Sanukehl Acne, Sanumgerman, Strophanthus Circulatory Problems in general, Alkala N, Leptospermusan, Leptucin, Mucokehl, Sankombi, Sanuvis Coeliac Disease, Exmykehl, Fortakehl, Mucokehl, Nigersan, Notakehl, Polysan Dx, Recarcin, Sanukehl Coli, Sanukehl Pseu, Sanukehl Salm, Sanukehl Staph Colds, Notakehl, Quentakehl, Polysan G, Relivora Komplex,Sanukehl Serra Colitis ulcerosa Syndrome, Albicansan, Exmykehl, Fortakehl, Latensin, Leptospermusan, Mucokehl, Nigersan, Notakehl, Rebas, Recarcin, Sanukehl Brucel, Sanukehl Cand, Sanukehl Coli, Sanukehl Myc, Utilin, Utilin S Collagen Diseases, Arthrokehlan A, Citrokehl, Fortakehl, Latensin, Sanukehl Pseu, Sanuvis Colon Cancer, (see also Cacinoma) Arthrokehlan A, Exmykehl, Fortakehl, Latensin, Mapurit, Mucokehl, Nigersan, Notakehl, Pefrakehl, Recarcin, Sanukehl Pseu, Sanuvis, Selenokehl, Utilin S Congestive Heart Failure, Calvakehl, Leptospermusan, Strophanthus Conjunctivitis, Citrokehl, Fortakehl, Leptospermusan, Luffasan, Mucokehl (eye drops), Notakehl, Ruberkehl, Sanukehl Myc, Sanuvis Constipation, Exmykehl, Fortakehl, Leptospermusan, Mucokehl, Sanukehl Cand, Utilin Convalescence, see recovery

349

Coronary Circulation Problems (see Artery Disease in general), Leptospermusan, Leptucin, Mapurit, Mucokehl, Sankombi, Sanukehl Acne, Strophanthus Corns and Calluses, Mucokehl, Notakehl, Sanuvis, Utilin Crohns Disease, Fortakehl, Latensin, Mucokehl, Nigersan, Polysan A, Recarcin, Sanukehl Brucel, Sanukehl Myc, Utilin S Cystitis, Citrokehl, Fortakehl, Leptucin, Notakehl, Pefrakehl, Ruberkehl, Sanukehl Coli, Sanukehl Myc, Sanuvis Dacryocystitis, Citrokehl, Mucokehl, Nigersan, Notakehl, Sanukehl Staph, Sanukehl Strep Degenerative Diseases of the Vertebrae and the Joints, Arthrokehlan A, Notakehl, Vitamin B Komplex Sanum N Dental Granuloma, Arthrokehlan U, Notakehl, Sankombi Dermatophytosis (Skin Fungal Infection), Albicansan, Fortakehl, Pefrakehl, Sanukehl Cand, Sanukehl Trich Diabetes Mellitus, Fortakehl, Grifokehl, Latensin, Mucokehl, Nigersan, Sankombi, Sanukehl Coli, Utilin, Utilin S, Zinkokehl Diabetic Gangrene, Leptucin, Mucokehl, Nigersan, Pinikehl, Sankombi, Sanukehl Acne, Utilin, Utilin S Diarrhea, Calvakehl, Exmykehl, Fortakehl, Nigersan, Okoubasan Dislocation, see distortions Distortions, Mucokehl, Sankombi, Sanuvis Diverticulitis, Fortakehl, Mucedokehl, Mucokehl, Notakehl, Sanukehl Myc, Sanukehl Pseu, Sanuvis Drug Abuse, Citrokehl, Mucedokehl, Muscarsan Dry Cough, Cerivikehl, Notakehl, Relivora Complex

Duodenal Ulcer, Fortakehl, Latensin, Recarcin, Sanukehl Myc, Sanukehl Prot, Utilin S Dupuytrens Contracture, Mucokehl, Nigersan, Polysan Dx, Utilin Dysbiosis, Albicansan, Citrokehl, Fortakehl, Notakehl, Pefrakehl, Sanukehl Myc, Sanukehl Prot, Sanuvis, Zinkokehl Dysfunction of the male Gonads from diseases or aging, Chrysocor, Citrokehl, Mucokehl, Nigersan, Sanuvis Dysmenorrhea, Chrysocor, Mucedokehl, Mucokehl, Nigersan, Recarcin, Sankombi, Ustilakehl, Utilin Ear Inflammation, see otitis Easy Fatigability, Bovisan, Citrokehl, Silvaysan Eczema, Latensin, Notakehl, Pefrakehl, Polysan T, Recarcin, Sankombi, Sanukehl Cand, Sanukehl Myc, Sanukehl Strep, Sanuvis, Utilin, Vitamin B Komplex Sanum N, Zinkokehl Elimination Therapy Luffasan, Okoubasan, Selenokehl, Usneabasan, Zinkokehl Embolism, Mucokehl, Sanukehl Acne, Sanuvis, Utilin S Empyema, Notakehl, Sanukehl Salm, Sanukehl Staph, Sanukehl Strep, UtilinS Encephalitis, Latensin, Notakehl, Quentakehl, Utilin, Utilin S Endocarditis, Mucokehl, Notakehl, Quentakehl, Sanukehl Staph, Sanukehl Strep, Utilin Endometritis, Alkala N, Calvakehl, Fortakehl, Mucokehl, Nigersan, Notakehl, Sanuvis Enteritis, Fortakehl, Okoubasan, Pefrakehl, Usneabasan, Utilin S Epicondylitis, Fortakehl, Mucokehl, Nigersan, Notakehl, Sanuvis, Utilin, Utilin S 350

Epididymitis, Citrokehl, Latensin, Mucokehl, Nigersan, Notakehl, Quentakehl, Sanukehl Coli, Sanukehl Myc Epilepsy, Mucedokehl, Mucokehl, Muscarsan, Nigersan, Sanumgerman, Utilin Erysipelas, Latensin, Notakehl, Quentakehl, Sanukehl Strep, Utilin Erythema nodosum, Bovisan, Sanukehl Strep, Utilin S Extrapulmonary Tuberculosis, Nigersan, Sanukehl Myc, Utilin S Exudative Erythema Multiforme, Nigersan, Utilin S Eye (Inflammation of), Mucokehl, Mucokehl (eye drops), Notakehl Femoral Artery and Vein Diseases, (see Artery Diseases in general) Mucokehl, Sanukehl Acne, Sanuvis Fever, Larifikehl, Notakehl, Polysan G, Quentakehl, Relivora Complex, Utilin S Fibromyalgia, Fortakehl, Latensin, Quentakehl, Sanukehl Myc, Sanukehl Pseu Fissures, see rhagades Folliculosis, Mapurit, Notakehl, Sanukehl Staph Food Poisoning, Okoubasan Fractures, Citrokehl, Mucokehl, Nigersan, Sanuvis, Utilin, Zinkokehl Frequent Infections, (see Susceptibility to Infection) Fortakehl, Sankombi, Utilin, Zinkokehl Frostbite, Leptucin, Mucokehl, Nigersan, Sanuvis, Utilin Full Sensation and Flatulence, Alkala N, Fortakehl, Pinikehl Functional Heart Complaints, Fortakehl, Mucokehl, Sanuvis, Strophanthus Fungal Infections in general, Albicansan, Exmykehl, Fortakehl, Nigersan, Notakehl, Pefrakehl, Sanukehl Cand

Furunculosis (Boils), Latensin, Mucokehl, Notakehl, Sanukehl Pseu, Sanukehl Salm, Sanukehl Staph, Utilin Gallbladder Disease, Alkala N, Fortakehl, Latensin, Pinikehl, Recarcin, Silvaysan, Utilin Ganglion Cyst, Latensin, Nigersan, Recarcin, Sankombi, Sanuvis, Utilin Gastric Mucosal Diseases, Alkala N, Fortakehl, Latensin, Recarcin, Sanukehl Prot Gastric Mucosal Inflammation, see gastritis Gastric Ulcer, Alkala N, Fortakehl, Latensin, Mucokehl, Recarcin, Sanukehl Myc, Sanukehl Prot, Sanuvis, Utilin Gastritis, Alkala N, Fortakehl, Latensin, Leptospermusan, Mucedokehl, Mucokehl, Recarcin, Sanukehl Myc, Sanukehl Prot, Sanuvis, Utilin Gastroenteritis, Citrokehl, Fortakehl, Latensin, Okoubasan, Pefrakehl, Sanukehl Coli, Sanukehl Salm Gastrointestinal Dysfunction, Citrokehl, Fortakehl, Pefrakehl, Pinikehl, Okoubasan, Sanuvis Gastrointestinal tract Disease, Alkala N, Calvakehl, Fortakehl, Latensin, Leptospermusan, Mucokehl, Rebas, Recarcin, Sanuvis, Utilin Gastrointestinal tract Infection, Fortakehl, Okoubasan, Quentakehl Gastrointestinal tract Inflammation, Fortakehl, Latensin, Recarcin, Sanukehl Prot Generalized Itchiness, (see Allergy in general) Fortakehl, Pefrakehl, Sanukehl Cand, Sanukehl Pseu, Sanuvis Genital Herpes, (see Herpes in general) Alkala N, Latensin, Mucokehl, Nigersan, Quentakehl, Sanukehl Prot, Stolonikehl Genital Itchiness, Albicansan, Alkala N, Fortakehl, Pefrakehl, Sanukehl Cand, Silvaysan

351

Genital Mycosis, (see mycosis in general) Albicansan, Exmykehl, Pefrakehl, Sanukehl Cand Gingivitis, Albicansan, Fortakehl, Latensin, Mucokehl, Nigersan, Notakehl, Pefrakehl, Sanukehl Cand, Utilin Glaucoma, Mucokehl, Mucokehl (eye drops), Sanuvis, Utilin S Gonorrhea, Notakehl, Polysan E, Utilin S Gout, Alkala N, Mucokehl, Recarcin, Sankombi, Sanuvis, Utilin Graves Disease (Exophtalmic Goiter), Latensin, Mucokehl, Nigersan, Notakehl, Sankombi, Utilin, Utilin S Growth and Developmental Disorders, Citrokehl, Fortakehl, Sanukehl Salm, Thymokehl Hair loss, (see Alopecia) Notakehl, Pleo Chelate, Sanukehl Myc, Sanukehl Trich, Selenokehl, Vitamin B Komplex Sanum N, Zinkokehl Hay Fever, (see Allergy in general) Luffasan, Ruberkehl, Sanukehl Pseu, Headache, see cephalgia Heartburn, Alkala N, Fortakehl, Sanukehl Myc, Sanukehl Strep, Strophanthus Heavy metal burden, Mapurit, Okoubasan, Pleo Chelate, Selenokehl, Usneabasan, Zinkokehl Hematoma (Bruises), Mucokehl, Sanuvis Hemiplegia, Leptucin, Mucokehl, Sankombi, Sanukehl Acne, Sanuvis, Utilin Hemorrhagic Rhinitis, Calvakehl, Mucokehl, Sanuvis, Ustilakehl Hemorrhoids, Mucokehl, Notakehl, Sanuvis Hepatitis B, Fortakehl, Leptucin, Pinikehl, Rebas, Sankombi, Silvaysan, Utilin

Herpes in general, Latensin, Notakehl, Quentakehl, Sankombi, Sanukehl Prot, Stolonikehl, Vitamin B Komplex Sanum N Herpes zoster, Notakehl, Quentakehl, Sanukehl Prot, Sanuvis, Stolonikehl, Vitamin B Komplex Sanum N Hodgkins Lymphogranulomatosis, Latensin, Mucokehl, Nigersan, Notakehl, Sanukehl Pseu, Sanuvis, Utilin Hydrocoele, Nigersan, Notakehl, Sanukehl Myc Hyperlipidemia, Lipiscor, Mucokehl, Nigersan, Sanuvis Hypertension, Lipiscor, Mucokehl, Utilin, Sanoryzae, Sanuvis Hyperthyroidism, Mucokehl, Nigersan, Notakehl, Sankombi, Utilin, Utilin S Hyperthrophy of the Tonsils, Bovisan, Mucokehl, Nigersan, Notakehl Hypogonadism, Chrysocor, Citrokehl, Mucokehl, Nigersan Hypotension, Mucokehl, Polysan K, Selenokehl, Utilin S Hypoxia, Calvakehl Ichthyosis (Dry scaly skin), Nigersan, Notakehl, Sankombi, Sanuvis, Utilin, Utilin S Immunomodulation, Arthrokehlan U, Bovisan, Episcorit, Fomepikehl, Grifokehl, Latensin, Leptucin, Recarcin, Relivora Complex, Sanukehl Pseu, Utilin, Utilin S Impetigo, Latensin, Notakehl, Sanukehl Staph, Utilin, Utilin S Induratio peninis, Mucokehl, Nigersan, Sanuvis Infarct, Status post Leptucin, Mucokehl, Sankombi, Sanukehl Acne, Sanukehl Strep, Sanuvis Infectious Diseases, Alkala N, Fortakehl, Notakehl, Quentakehl, Sanuvis

352

Infectious Skin Disease, Albicansan, Notakehl, Pefrakehl, Sanuvis, Utilin I n f e r t i l i t y , Chrysocor, Fortakehl, Latensin, Mucokehl, Nigersan, Sankombi, Sanuvis, Selenokehl Inflammation after BCG Vaccination, Bovisan, Citrokehl, Nigersan Inflammation in general, Latensin, Leptospermusan, Mucokehl, Notakehl, Polysan G, Rebas Inflammation of the Biliary Tract, Citrokehl, Fortakehl, Latensin, Mucokehl, Notakehl, Pinikehl, Sanukehl Coli, Sanukehl Myc, Utilin Inflammation of the Digestive Organs, (see gastritis, Crohns disease, Colitis ulcerosa) Fortakehl, Larifikehl, Latensin, Mucokehl, Sanukehl Myc, Sanukehl Pseu, Sanuvis, Utilin Inflammatory Process of the Stomach, Citrokehl, Cuprukehl, Fortakehl, Latensin, Notakehl, Recarcin, Sanukehl Prot Influenza Infection, Polysan G, Quentakehl, Ruberkehl, Sanukehl Klebs, Sanuvis Inherited Toxins, Polysan E, Utilin S Insect Bites, Notakehl, Sankombi, Sanukehl Pseu, Sanuvis Intercostal Neuralgia, Citrokehl, Notakehl, Quentakehl, Sanuvis, Stolonikehl Intermittent Claudication, see smokers Leg Intermittent Fever, Pinikehl, Polysan M, Sanukehl Brucel Intestinal Dysfunction, Fortakehl, Utilin Intestinal Yeast Infection, Albicansan, Exmykehl, Fortakehl, Pefrakehl, Sanukehl Cand Intestinal Tuberculosis, Citrokehl, Latensin, Nigersan, Sanukehl Myc, Utilin S Intoxication, Okoubasan

Iridocyclitis, Mucokehl, Nigersan, Notakehl, Sanuvis Joint Diseases, Latensin, Notakehl, Recarcin, Sanukehl Strep Keloid, Mucokehl, Sanukehl Pseu Keratitis, Mucokehl, Sanukehl Myc Kraurosis Vulvae, Citrokehl, Nigersan, Sanukehl Myc Landry Palsy (Guillian Barr Syndrome), Exmykehl, Lipiscor, Notakehl, Quentakehl, Sankombi, Utilin S, Vitamin B Komplex Sanum N Large Intestinal Inflammation, see colitis ulcerosa Laryngeal Ulceration, Notakehl, Quentakehl, Recarcin, Sanukehl Myc Laryngitis, Cerivikehl, Nigersan, Notakehl, Quentakehl Leg Cramps, Latensin, Mapurit, Mucokehl Leukemia, Citrokehl, Mucokehl, Nigersan, Sankombi, Sanuvis Leukopenia, Latensin, Mucokehl, Nigersan, Pinikehl, Sanukehl Pseu, Sanuvis Libido Problems, Chrysocor, Citrokehl, Ginkgobakehl, Mapurit, Nigersan, Selenokehl Lichen ruber (Acuminatus Pityriasis), Latensin, Mucokehl, Nigersan, Sanukehl Trich, Sanuvis, Utilin, Zinkokehl Lipomatosis, Lipomas Citrokehl, Latensin, Lipiscor, Mucokehl, Nigersan, Recarcin, Sanuvis, Utilin S Liver Cancer, (see Carcinoma) Chrysocor, Exmykehl, Latensin, Lipiscor, Mucokehl, Nigersan, Recarcin, Sanukehl Pseu, Sanuvis Liver Cirrhosis, Citrokehl, Mucokehl, Nigersan, Notakehl, Pinikehl, Recarcin, Sanuvis, Silvaysan Liver Disease, Alkala N, Latensin, Notakehl, Pinikehl, Rebas, Sankombi, Sanuvis, Silvaysan, Utilin

353

Liver Parenchymal Disorder, Sankombi, Selenokehl, Silvaysan, Utilin Lobar Pneumonia, (see Pneumonia in general) Citrokehl, Fortakehl, Nigersan, Notakehl, Polysan Dx, Polysan T, Sanukehl Klebs, Sanukehl Staph Low Energy/Performance Levels, Chrysocor, Citrokehl, Mapurit, Selenokehl Lumbago, Notakehl, Nigersan, Recarcin, Utilin, Vitamin B Komplex Sanum N Lung Abscess, Larifikehl, Mucokehl, Notakehl, Sanukehl Myc, Sanukehl Pseu Lung Cancer, Fortakehl, Mucokehl, Nigersan, Notakehl, Pefrakehl, Recarcin, Sankombi, Sanukehl Myc, Sanukehl Pseu, Sanuvis, Utilin S Lung Diseases, Cerivikehl, Citrokehl, Larifikehl, Nigersan, Notakehl, Utilin S Lung Emphysema, Fortakehl, Larifikehl, Latensin, Mucokehl, Nigersan, Sanukehl Myc, Utilin Lupus, Fortakehl, Latensin, Mucokehl, Nigersan, Pefrakehl, Recarcin, Sanukehl Myc, Sanuvis, Utilin, Utilin S Lyme Borreliose Alkala N, Fortakehl, Mucokehl, Nigersan, Notakehl, Sanukehl Brucel, Utilin S Lymphadenitis (Lymph Node Swelling), Latensin, Mucokehl, Nigersan, Notakehl, Pefrakehl, Recarcin, Sanoryzae, Sanuvis, Utilin S Lymphatic Constitution, Nigersan, Pefrakehl, Sankombi, Sanoryzae, Sanuvis Lymphoma, Latensin, Mucokehl, Nigersan, Sankombi, Utilin Lymphostasis, Mucedokehl, Mucokehl, Nigersan Magnesium Deficiency (Malabsorbtion), Mapurit

Malaria, Status Post Citrokehl, Fortakehl, Mucokehl, Nigersan, Notakehl, Polysan M, Sanukehl Brucel, Sanuvis, Utilin S Male menopausal Syndrome, Alkala N, Chrysocor, Mucedokehl, Nigersan, Sanuvis, Silvaysan Malignant Melanoma, see carcinoma Mastitis Mucokehl, Notakehl, Sanukehl Staph, Sanukehl Strep Mastoiditis, Mucokehl, Nigersan, Notakehl, Sanukehl Staph Measles, Notakehl, Quentakehl, Utilin Menires Disease, Mucokehl, Quentakehl, Sanukehl Prot Meningitis, Latensin, Notakehl, Quentakehl, Sanukehl Staph, Sanukehl Strep, Utilin S Menopausal Symptoms, Mucokehl, Sankombi, Ustilakehl, Utilin Menorrhagia (Excessive Menstruation), Calvakehl, Ustilakehl Metabolic Disorders, Citrokehl, Mapurit, Polysan A, Sanuvis, Selenokehl, Silvaysan Metritis (Inflammation of the Uterus), Fortakehl, Notakehl, Sankombi, Sanukehl Coli, Sanukehl Myc Metrorrhagia (Uterine Bleeding), Calvakehl, Ustilakehl Middle Ear Infections, see otitis media Migraine, Alkala N, Latensin, Leptospermusan, Luffasan, Mucokehl, Quentakehl, Polysan T, Sanukehl Strep, Sanuvis, Selenokehl, Silvaysan, Usneabasan, Ustilakehl Mouth Diseases, Albicansan, Notakehl, Pefrakehl, Sanukehl Cand, Sanukehl Myc

354

Multiple Sclerosis, Exmykehl, Latensin, Mucokehl, Nigersan, Notakehl, Pleo Chelate, Quentakehl, Recarcin, Sanumgerman, Sanuvis, Stolonikehl, Utilin Myalgia (Muscle Pains), Arthrokehlan A, Larifikehl, Mapurit, Sanukehl Brucel, Sanuvis, Vitamin B Komplex Sanum N Mycosis in general, Albicansan, Exmykehl, Nigersan, Notakehl, Sankombi, Pefrakehl, Sanukehl Cand Myocardial Infarction, Alkala N, Leptospermusan, Mucokehl, Sanukehl Acne, Sanuvis Myocarditis, Mucokehl, Notakehl, Quentakehl, Sanukehl Strep Nasal Mucosa Inflammation, Luffasan, Mucedokehl, Notakehl, Quentakehl, Recarcin, Ruberkehl Nephritis, Cuprukehl, Latensin, Mucokehl, Nigersan, Notakehl, Quentakehl, Ruberkehl, Sankombi, Sanukehl Myc, Sanukehl Staph, Sanuvis, Utilin Nephroses, Latensin, Notakehl, Pefrakehl, Quentakehl, Ruberkehl, Sanuvis Nerve Inflammation, see neuritis Neuralgia, Mapurit, Notakehl, Polysan R, Quentakehl, Selenokehl, Vitamin B Komplex Sanum N Neurodermatitis, Fortakehl, Latensin, Mucokehl, Nigersan, Notakehl, Sanuvis, Utilin, Utilin S Neuromuscular Disorders, Cerivikehl, Latensin, Mapurit, Okoubasan Neuropathy, Mucedokehl, Notakehl, Polysan A, Sanukehl Acne, Selenokehl, Stolonikehl Neuritis, Mapurit, Mucokehl, Notakehl, Recarcin, Sankombi, Utilin, Utilin S, Vitamin B Komplex Sanum N, Zinkokehl No appetite, Cerivikehl, Citrokehl, Fortakehl

Nodules, Sanukehl Coli, Utilin Nose Bleeding, Calvakehl Obesity, Alkala N, Grifokehl, Latensin, Mucedokehl, Muscarsan, Nigersan, Utilin, Utilin S Oophoritis (Inflammation of the Ovaries), Mucokehl, Notakehl, Quentakehl, Recarcin Osteochondritis, Citrokehl, Latensin, Nigersan, Notakehl, Utilin Osteochondrosis, Latensin, Nigersan, Notakehl, Sanukehl Myc, Utilin S Osteomyelitis, Mucokehl, Notakehl, Quentakehl, Sanukehl Prot, Sanukehl Staph, Sanukehl Strep, Utilin S Osteoporosis, Alkala N, Citrokehl, Fortakehl, Latensin, Nigersan, Recarcin, Sankombi, Sanuvis, Utilin O s t i t i s , Citrokehl, Mucedokehl, Mucokehl, Notakehl, Sankombi, Sanuvis, Utilin Otitis Externa, Notakehl, Pefrakehl Otitis Media, Mucokehl, Nigersan, Notakehl, Recarcin, Sanukehl Pseu, Sanukehl Strep, Sankombi, Utilin Otosclerosis, Citrokehl, Mucokehl, Nigersan, Polysan E, Utilin Ovarian Cyst, Citrokehl, Mucokehl, Nigersan, Utilin, Utilin S Pancreatic Insufficiency, Alkala N, Citrokehl, Fortakehl, Nigersan, Pinikehl, Silvaysan Pancreatitis, Fortakehl, Mucokehl, Nigersan, Notakehl, Quentakehl, Recarcin, Sanuvis, Zinkokehl Paradentosis, Citrokehl, Nigersan, Notakehl, Pefrakehl, Pleo Chelate, Polysan A

355

Paratubercular Inflammation, Bovisan, Fortakehl, Nigersan, Sankombi, Utilin Parkinsons Disease, Fortakehl, Latensin, Leptucin, Mapurit, Mucedokehl, Mucokehl, Nigersan, Sanukehl Acne, Utilin Pemphigus Vulgaris, Mucokehl, Pefrakehl, Quentakehl, Utilin S Perianal Eczema, Pefrakehl, Utilin, Albicansan Pericarditis, Mucokehl, Notakehl, Quentakehl, Sanukehl Strep, Strophanthus Peripheral Vascular Disease, Ginkgobakehl, Leptospermusan, Leptucin, Mucokehl, Sanukehl Acne, Sanukehl Prot Peritonsillitis, Notakehl, Sanukehl Prot Pernicious Anemia, Fortakehl, Mucokehl, Sanuvis, Utilin, Vitamin B Komplex Sanum N Perthess Disease, Citrokehl, Latensin, Nigersan, Utilin Pertussis, Quentakehl, Recarcin, Relivora Complex, Ruberkehl Peyronies Disease, see Induratio peninis Pharyngitis, Notakehl, Quentakehl, Sanukehl Pseu, Utilin S pH regulation, Alkala N, Citrokehl, Sanuvis Pleuritis, Nigersan, Notakehl, Sanukehl Myc, Sanukehl Klebs Pneumoconiosis, Notakehl, Sanukehl Klebs Pneumonia, Citrokehl, Nigersan, Notakehl, Sanukehl Coli, Sanukehl Klebs, Sanukehl Staph, Sanukehl Strep, Utilin Polyarthritis, Larifikehl, Mucokehl, Nigersan, Notakehl, Recarcin, Sanukehl Brucel, Sanukehl Myc, Sanuvis, Utilin S

Poor Bone and Cartilage Growth and Healing, Nigersan, Selenokehl, Utilin, Zinkokehl Post Alcohol Abuse, Muscarsan, Alkala N, Mucedokehl, Citrokehl Post Menopausal Syndrome, Chrysocor, Ustilakehl, Utilin Precancerous stages, Fortakehl, Mapurit, Polysan Om, Sanukehl Pseu, Selenokehl, Utilin S, Zinkokehl Pre- and Post-operative Phase, Chrysocor, Cuprukehl, Mucokehl, Sanuvis Pregnancy, Sankombi, Sanuvis Problems of the Elderly, Chrysocor, Citrokehl, Latensin, Mucokehl, Nigersan, Polysan A, Sankombi, Sanuvis, Selenokehl, Utilin Progressive Chronic Polyarthritis, see rheumatoid arthritis Prostatic Adenoma and Hypertrophy, Exmykehl, Fomepikehl, Mucokehl, Nigersan, Notakehl, Sanuvis Prostatic Cancer, Exmykehl, Fomepikehl, Mucokehl, Nigersan, Notakehl, Sankombi, Sanukehl Pseu Prostatitis, Exmykehl, Mucokehl, Nigersan, Notakehl, Pefrakehl, Polysan A, Sanukehl Coli Psoriasis, Fortakehl, Latensin, Mucokehl, Notakehl, Recarcin, Sanukehl Myc, Sanuvis, Utilin, Utilin S Psoriatic Arthritis, Fortakehl, Larifikehl, Latensin, Recarcin, Utilin S, Zinkokehl Puerperal Sepsis, Notakehl, Sanukehl Prot, Sanukehl Pseu Pyelocystitis and -nephritis, Citrokehl, Nigersan, Notakehl, Sanukehl Coli, Sanukehl Myc, Sanukehl Prot, Sanuvis Pyloric Spasm, Fortakehl, Leptospermusan, Mucedokehl Pyoderma, Mucokehl, Notakehl, Pefrakehl, Sankombi, Utilin Raynauds disease, Leptucin, Mucokehl, Sanukehl Acne, Sanuvis

356

Recovery, Latensin, Mucokehl, Zinkokehl Rectal Cancer, see Carcinoma Reiters Disease, Fortakehl, Latensin, Mucokehl, Notakehl, Recarcin, Utilin Respiratory Diseases, Alkala N, Cerivikehl, Citrokehl, Formasan, Latensin, Luffasan, Mucedokehl, Notakehl, Sankombi, Sanukehl Klebs Respiratory Inflammation, Notakehl, Quentakehl, Relivora Complex Rheumatic Fever, (see Rheumatism) Fortakehl, Notakehl, Sanukehl Salm Rheumatism, Alkala N, Arthrokehlan A, Bovisan, Citrokehl, Latensin, Mucokehl, Nigersan, Polysan R, Polysan T, Recarcin, Sankombi, Utilin, Utilin S, Vitamin B Komplex Sanum N Rheumatoid Arthritis, Fortakehl, Latensin, Nigersan, Notakehl, Recarcin, Sanukehl Acne, Utilin, Vitamin B Komplex Sanum N, Zinkokehl Rhinitis, Fortakehl, Latensin, Luffasan, Mucokehl, Nigersan, Quentakehl, Recarcin, Ruberkehl, Sanukehl Myc, Sanuvis, Utilin Salpingitis, Notakehl, Sanukehl Coli Scarlet Fever, Mucokehl, Notakehl, Sanukehl Strep, Utilin Scheuermanns Disease, Citrokehl, Latensin, Mucokehl, Nigersan, Sanuvis Sciatica (Sciatic Nerve Pain), Mucokehl, Notakehl, Utilin, Vitamin B Komplex Sanum N Scintillating Scotoma, Mucokehl (eye drops) Septic Fever, Alkala N, Citrokehl, Fortakehl, Nigersan, Notakehl, Pefrakehl, Pinikehl, Quentakehl, Sanuvis Silicosis, Citrokehl, Mucokehl, Nigersan, Sanukehl Klebs

Sinubronchitis, Fortakehl, Latensin, Mucedokehl, Nigersan, Notakehl Sinusitis, Cerivikehl, Luffasan, Mucedokehl, Notakehl, Pinikehl, Quentakehl, Ruberkehl, Sanukehl Pseu, Sanukehl Staph, Utilin S Skin and Conjunctival Tuberculosis, Nigersan, Sanukehl Acne, Utilin S Skin Diseases, Calvakehl, Pefrakehl, Sanuvis, Utilin, Zinkokehl, Sleep Disturbance, Fortakehl, Leptospermusan Smokers Leg, Leptucin, Mucokehl, Sanukehl Acne, Sanuvis Spherocytosis, Fortakehl, Mucokehl, Nigersan, Pefrakehl, Vitamin B Komplex Sanum N Spleen Diseases, Mucokehl, Okoubasan, Pinikehl, Sanuvis Spondylopathy, Citrokehl, Latensin, Nigersan, Notakehl, Quentakehl Sprains, Mucokehl Stimulation of Blood Cells Production, Citrokehl, Leptucin, Mucokehl, Sanuvis Stomatitis, Albicansan, Notakehl, Pefrakehl, Quentakehl, Recarcin, Sanukehl Cand, Utilin Stroke, Leptospermusan, Leptucin, Mucokehl, Sanukehl Acne, Sanuvis, Utilin Stye, Notakehl, Sanukehl Myc, Sanukehl Staph Sunstroke, Usneabasan Suppurations, Notakehl, Polysan G Susceptibility to Infection, Fortakehl, Quentakehl, Sankombi, Sanukehl Serra, Utilin S Symbiotic Therapy (Symbiosis), (see Dysbiosis) Fortakehl, Pefrakehl, Sanukehl Coli

357

Swelling, Mucokehl, Sanuvis Tennis Elbow, see epicondylitis Tension Headaches, Muscarsan, Quentakehl, Usneabasan Thromboangiitis obliterans (Buergers disease), Citrokehl, Mucokehl, Nigersan, Notakehl, Sanuvis, Utilin S Thrombophlebitis, Mucokehl, Notakehl, Sanukehl Myc, Sanuvis, Utilin Thrombosis, Mucokehl, Sanuvis, Utilin, Zinkokehl Thyroid Disease and Dysfunction, Citrokehl, Fortakehl, Latensin, Mucedokehl, Nigersan, Pleo Chelate, Recarcin, Sanukehl Myc, Sanukehl Prot, Sanuvis, Utilin,Utilin S Tinea, Pefrakehl, Sanukehl Trich Tinnitus, Citrokehl, Latensin, Leptucin, Mucokehl, Nigersan, Notakehl, Sanuvis, Utilin Tonsillitis, Mucedokehl, Notakehl, Polysan G, Sankombi, Sanukehl Staph, Sanukehl Strep, Utilin Tooth Abscess, Arthrokehlan A, Notakehl Transient Ischemic Attacks, Alkala N, Mucokehl, Leptospermusan, Sanuvis Trichomycosis (Fungal infection of the hair) and Trichophytosis (Tinea barbae), Notakehl, Pefrakehl, Sankombi, Sanukehl Trich, Utilin S Trigeminal Neuralgia, Leptospermusan, Stolonikehl, Vitamin B Komplex Sanum N Tubal Cyst, Citrokehl, Mucokehl, Nigersan, Utilin Tubercular Rheumatism, Bovisan, Citrokehl, Nigersan, Sanumgerman, Utilin S Tuberculoid Skin Problem, Citrokehl, Nigersan, Polysan T, Utilin, Utilin S

Tuberculosis in general, Bovisan, Chrysocor, Citrokehl, Latensin, Nigersan, Polysan T, Sanukehl Myc, Utilin, Utilin S Tumors, see Carcinoma Ulcus cruris, Leptucin, Mucokehl, Notakehl, Sanukehl Myc, Sanukehl Pseu, Sanuvis, Zinkokehl Upper Abdominal Complaints, Fortakehl, Latensin, Mucokehl, Recarcin, Utilin S Urethritis, Albicansan, Mucokehl, Nigersan, Notakehl, Pefrakehl, Sanukehl Staph, Sanukehl Myc Urinary tract infection, Fortakehl, Latensin, Nigersan, Notakehl, Pefrakehl, Sanukehl Coli, Sanukehl Myc Urticaria, Formasan, Fortakehl, Latensin, Mucokehl, Nigersan, Sanukehl Myc, Sanuvis, Utilin, Utilin S Uterine Bleeding, Calvakehl, Ustilakehl Uterine Myoma, Mucokehl, Nigersan, Selenokehl, Utilin S Vaginal Discharge, Albicansan, Notakehl, Pefrakehl, Sankombi, Recarcin, Sanuvis Vaginitis, Albicansan, Grifokehl, Notakehl, Pefrakehl, Quentakehl, Sanukehl Cand, Sanukehl Coli, Sanukehl Myc Varicose Veins, Mucokehl, Nigersan, Polysan K, Sanuvis Vascular Migraine, Leptospermusan, Leptucin, Quentakehl, Sanoryzae, Selenokehl Vascular System Complaints, Mucokehl Veins Diseases, Mucokehl, Polysan K, Sankombi, Zinkokehl Vertigo, Luffasan, Mucokehl, Quentakehl V i t i l i g o , Citrokehl, Mucokehl, Nigersan, Sanuvis, Utilin S

358

Viral Infections, Citrokehl, Grifokehl, Leptospermusan, Notakehl, Quentakehl, Sanuvis Vitamin E Deficiency, Mapurit Vomiting, Fortakehl Vomiting of blood, Calvakehl, Fortakehl, Sanukehl Prot Vulvovaginitis, Albicansan, Notakehl, Pefrakehl, Quentakehl, Sanukehl Cand

Warts, Citrokehl, Latensin, Mucokehl, Nigersan, Sanuvis, Utilin S Weak Immune System, see Immunomodulation Whooping Cough, see Pertussis Wound Healing Problems, Mucokehl, Sankombi, Zinkokehl Yeast Infection of the Vagina, Albicansan, Alkala N, Citrokehl, Exmykehl, Fortakehl, Pefrakehl, Recarcin, Sanukehl Cand

359