Active substanceEleutherococcus spiny rhizome and rootsEleutherococcus spiny rhizome and roots
Dosage form: & nbspextract for oral administration [liquid]
Composition:

To obtain the extract, use:

Active substance:

Rhizome and root of Eleutherococcus prickly - 1000 g

Excipient:

Ethanol (ethyl alcohol) 40% - to obtain 1000 ml of extract
Description:A liquid of a dark brown color with possible easy opalescence and a peculiar smell. During storage, a precipitate may form.
Pharmacotherapeutic group:tonic
ATX: & nbsp

A.13.A   Tetanus preparations

Pharmacodynamics:It has a stimulating effect on the central nervous system, tonic and restorative effect on the body, increases the general nonspecific resistance of the organism, improves appetite, improves physical and mental performance
Indications:Mental and physical fatigue, asthenic conditions of various etiologies, arterial hypotension (low blood pressure), neurasthenia, recovery period after infectious diseases and postoperative period
Contraindications:

Increased individual sensitivity to the components of the drug,hypertension (high blood pressure), heart rhythm disturbance, myocardial infarction, cerebrovascular pathology, increased excitability, epilepsy, convulsions, insomnia, acute infectious diseases, chronic liver disease, pregnancy, the period of breastfeeding, children under 12 years.

Carefully:

Alcoholism, craniocerebral trauma, brain disease, children's age from 12 years.

Dosing and Administration:

The drug is used inside, before meals, in the morning. Adults appoint 20-30 drops 2-3 times a day. Children over 12 years - in a dose of 1 drop per year of life. The course of treatment is 25-30 days. If necessary, repeat courses with two-week breaks (or without them) after consulting a doctor.

Shake before use
Side effects:

Possible allergic reactions, insomnia, hypoglycemia, headache, tachycardia.

Overdose:When using the drug in doses exceeding the recommended dose, it is possible to increase dose-related side effects. Treatment: symptomatic
Interaction:

Strengthens the action of stimulants of the central nervous system, is an antagonist of drugs that depress the central nervous system (including neuroleptics, barbiturates, anxiolytics, antiepileptic drugs).

With simultaneous use with digoxin, an increase in the concentration in the blood plasma of the latter is possible; with hypoglycemic drugs (including insulin) and anticoagulants may enhance the effect.

Special instructions:

The drug should not be taken in the afternoon to avoid sleep disturbances. When hypoglycemia occurs, it is recommended to reduce the dose of the drug, take it after a meal or cancel the drug.

The maximum single dose of the drug (30 drops) contains 0.47 grams of absolute ethyl alcohol, the maximum daily dose of the drug (90 drops) -1.41 grams of absolute ethyl alcohol.

Effect on the ability to drive transp. cf. and fur:During drug treatment, care should be taken when carrying out potentially dangerous activities requiring increased concentration and speed of psychomotor reactions (vehicle management, working with moving mechanisms,work of the dispatcher and the operator).
Form release / dosage:

Extract for oral administration [liquid].

Packaging:

For 25 and 50 ml in bottles of droppers of orange glass or in bottles of orange glass or in bottles with a screw mouth of brown glass, sealed with stoppers-droppers polymer or polymer caps and polymeric caps screwed, or lids with a dropper.

Each vial or dropper along with the instruction for use is placed in a pack of cardboard.

Packing for hospitals.

By 4, 9 or 17 kg in cans of polyethylene with lids.

For 17 kg in a glass bottle, sealed with polymeric screw caps with polyethylene gaskets. Each bottle is placed in a polyethylene drum for glass bottles.

Storage conditions:

Store in a dark place at a temperature of 15 to 25 ° C.

Keep out of the reach of children
Shelf life:

4 years.

Do not use the drug after the expiration date.

Terms of leave from pharmacies:Without recipe
Registration number:LSR-002484/07
Date of registration:28.08.2007
The owner of the registration certificate:MOSCOW PHARMACEUTICAL FACTORY, CJSC MOSCOW PHARMACEUTICAL FACTORY, CJSC Russia
Manufacturer: & nbsp
Information update date: & nbsp21.10.2015
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