Universal reference book for medicines
Product name: KEDROVIT

Active substance: comb.
drug
Type: Phytopreparation with restorative action

Manufacturer: МЕЛ�ГЕН ФП (Russia)
Composition, form of production and packaging
?
Elixir in the form of a liquid of brown color, with a specific smell; in the course of storage, precipitation may occur.
1 l

seeds of pine cedar Siberian 54 g

hawthorn fruit 4 g

fruits of chokeberry aronia 2 g

birch buds 1.5 g

rhizomes with roots of eleutherococcus 1 g

flowers of hawthorn 0.5 g

Excipients: honey natural - 50 g, sucrose - 22.7 g, ethanol 95% - 421 g, purified water - up to 1000 ml.

100 ml - glass bottles (1) - packs of cardboard.

250 ml - bottles of glass (1) - packs of cardboard.

INSTRUCTION FOR THE SPECIALIST.

Description of the drug approved by the manufacturer for the printed edition of 2015.

PHARMACHOLOGIC EFFECT

It has a general strengthening effect, increases physical efficiency, promotes the regulation of metabolic processes in the body.

PHARMACOKINETICS

The drug is a water-alcohol extract from a mixture of herbal medicinal raw materials and contains a complex of biologically active substances, and therefore, the conduct of pharmacokinetic studies is not possible.

INDICATIONS

- for the treatment of asthenic-vegetative syndrome of various etiologies, in the period of recovery after the transferred diseases, proceeding with the defeat of parenchymal organs.

DOSING MODE

Inside for 2-3 teaspoons (10-15 ml), diluted in 100 ml of water.
2 times a day for 10-15 minutes before meals. The course of treatment is 5-7 days. If necessary, the course of treatment can be increased to 2-3 weeks after consulting a doctor. Shake before use.
SIDE EFFECT

Allergic reactions are possible.

If, on the background of taking the drug, your condition worsens, and you notice any side effects not listed in this manual, contact your doctor.

CONTRAINDICATIONS

- Hypersensitivity to the components of the drug, including honey and bee products;

- acute cardiovascular and acute renal failure;

- severe liver disease;

- Alcoholism;

- craniocerebral trauma;

- diseases of the brain;

- deficiency of sugar / isomaltase;

- intolerance to fructose;

- glucose-galactose malabsorption;

- age to 18 years.

PREGNANCY AND LACTATION

The use of the drug during pregnancy and during breastfeeding is contraindicated.

APPLICATION FOR FUNCTIONS OF THE LIVER

Contraindicated in acute renal failure.

APPLICATION FOR VIOLATIONS OF THE FUNCTION OF KIDNEYS

Contraindicated in severe liver disease.

APPLICATION FOR CHILDREN

Contraindicated for children under 18 years.

SPECIAL INSTRUCTIONS

The composition of the drug contains sucrose, which should be taken into account by a patient with diabetes mellitus.
The maximum single dose of the preparation contains 0.34 g of sucrose (corresponding to 0.3 XE (bread units)), daily 0.68 g (corresponding to 0.68 XE).
The preparation contains not less than 37% of ethyl alcohol.
The maximum single dose of the drug contains 5.9 grams of absolute ethyl alcohol, the maximum daily dose of the drug contains 11.97 grams of absolute ethyl alcohol.
Influence on ability to drive vehicles and work with mechanisms

Due to the presence of ethyl alcohol in the drug, one should refrain from potentially dangerous activities requiring increased concentration of attention and speed of psychomotor reactions (vehicle management, work with moving mechanisms, dispatcher, operator, etc.).

OVERDOSE

When using the drug in doses exceeding the recommended, you may have a headache, nausea, vomiting.
Treatment is symptomatic.
DRUG INTERACTION

When used simultaneously with nicotinic acid, lipid-lowering agents (cholesterol absorption inhibitors, fibrates), an increase in hypolipidemic action is possible.

If you are taking other medications, always consult a doctor before taking the drug.

TERMS OF RELEASE FROM PHARMACY

Without recipe.

TERMS AND CONDITIONS OF STORAGE

At a temperature of 15 to 25 В° C, in a place protected from light.
Keep out of the reach of children. Shelf life - 3 years.
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