Befungin 100 ml
Composition
1 bottle (jar) 100 ml/ml contains liquid chaga extract (1:1) - 85 g/g, ethyl alcohol 96% - 7 g/g, cobalt sulfate heptahydrate - 0.001 g/g, purified water - up to 100 ml/ml.
Pharmacological properties
The action of a dietary supplement is determined by the effect of the biologically active substances that make up its composition.
Birch mushroom (chaga) (Inonotus obliquus) is a source of natural biologically active substances, trace elements (potassium, iron, copper, calcium, manganese, magnesium, sodium, silicon, zinc), formic, acetic, butyric, vanillic, paraoxybenzoic acids, two triterpenic acids from the group of tetracyclic triterpenes, obliquinic, humic chaga, iononotic, etc., as well as free phenols, polysaccharides, pterins, lignin, fiber, sterols - ergosterol, lanosterol, inotodiol. The main active substances are pigments that form a chromogenic polyphenolcarbon complex (20%) in combination with polysaccharides (6-8%), agaricic and humic chaga acids.
Befunginum/Befungin activates metabolism and basic physiological processes, enhances the general nonspecific resistance of the body, specific and nonspecific mechanisms of immunological protection. It has antiproliferative (cytostatic), immunomodulatory, antibacterial (antiviral), anti-inflammatory, antioxidant, reparative, analgesic, antispasmodic, laxative effects. It has pronounced gastroprotective properties, eliminates dyspeptic phenomena, activates intestinal motility, reduces blood sugar levels in people with diabetes, acts as a general strengthening and tonic.
The presence of copper, manganese, and cobalt provides a stimulating effect on hematopoiesis, especially leukopoiesis.
Indications for use
Befunginum/Befungin is prescribed as an adjunct in the complex therapy of chronic gastritis, gastric ulcer and duodenal ulcer without exacerbation, intestinal dyskinesia of the hypotonic type (including constipation), chronic hepatitis (including conditions accompanied by fatty infiltration of the liver), Crohn's disease, obesity, psoriasis, neurodermatoses, eczema, acne, warts, prostate adenoma, as well as a symptomatic remedy that improves the general condition of cancer patients.
Contraindication
Pregnancy, breastfeeding, children under 18 years of age. Hypersensitivity (intolerance) to any of the components of Befunginum/Befungin.
Interaction with other tools and other types of interaction
Should not be administered with antibiotics or simultaneous administration of glucose (dextrose).
Side effect
Dyspeptic symptoms and allergic reactions (itching of the skin) may rarely occur.
If any adverse reactions occur, discontinue use and consult a doctor immediately.
Reservation
Contains ethanol (alcohol).
Harmful for patients suffering from alcoholism. Caution should be exercised when used in patients with liver disease and epilepsy.
When using Befunginum, it is recommended to follow a lactic acid diet with a restriction (exclusion) of animal fats, smoked meats, canned food, and spicy seasonings.
During storage, sedimentation is allowed, so it must be shaken before use.
Ability to influence the reaction rate when driving vehicles or other mechanisms. The effect of the drug on the ability to drive vehicles or work with complex mechanisms is unknown.
Do not exceed the recommended daily intake. Do not use as a substitute for a balanced diet.
Overdose
There are no data on overdose in humans. Specific antidote is unknown.
In case of overdose, use should be discontinued. Treatment is symptomatic.
Method of administration and doses
Befunginum/Befungin is to be taken orally. Dilute 3 teaspoons of concentrate in 150 ml/ml of warm boiled water and take 1 tablespoon 3 times a day 30 minutes before meals or 2 hours after meals.
The recommended duration of use is 3-5 months. If necessary, the course of use can be repeated after 7-10 days. It is recommended to conduct no more than 4 courses of administration during the year.
Storage conditions
In a dry, dark place, at a temperature not exceeding 25 °C and a relative humidity of 75%. Keep out of the reach of children.
Expiration date
2 years.
Not a medicine. Non-GMO. Requires consultation with a doctor before use.
Producer
PJSC "Biolik", Ukraine, 24321, Vinnytsia region, Ladyzhyn, 118 Nezalezhnosti St.
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