Clinical and pharmacological group: & nbsp

Genotoninizing agents and adaptogens

Included in the formulation
  • Eleutherococcus spiny rhizome and roots
    powderraw materials. inwards 
  • Eleutherococcus extract liquid
    extract inwards 
  • Eleutherococcus extract liquid
    extract inwards 
    BEGRIF, LTD     Russia
  • Eleutherococcus extract liquid
    extract inwards 
    MAKSFARM, OJSC     Russia
  • Eleutherococcus extract liquid
    extract inwards 
  • Eleutherococcus extract liquid
    extract inwards 
  • Eleutherococcus extract liquid
    extract inwards 
  • Eleutherococcus extract liquid
    extract inwards 
  • Eleutherococcus extract liquid
    extract inwards 
  • Eleutherococcus extract liquid
    extract inwards 
    CAMELIA NPP, LLC     Russia
  • Eleutherococcus extract liquid
    extract inwards 
    DALHIMFARM, OJSC     Russia
  • Eleutherococcus extract liquid
    extract inwards 
  • Eleutherococcus extract dry
    raw materials.extract inwards 
  • АТХ:

    A.13.A   Tetanus preparations

    Pharmacodynamics:

    Vegetable preparation; has an adaptogenic effect, increases the nonspecific resistance of the organism. Has a stimulating effect on the central nervous system, eliminates fatigue, irritability; restores and enhances physical and mental performance, protects from unfavorable environmental factors.

    Pharmacokinetics:

    Not described.

    Indications:

    Asthenia, neurasthenia; reconvalescence (after somatic and infectious diseases); arterial hypotension, mental and physical overwork.

    V.F40-F48.F48.0   Neurasthenia

    IX.I95-I99.I95   Hypotension

    XXI.Z40-Z54.Z54   Condition of recovery

    XXI.Z70-Z76.Z73.0   Overwork

    XXI.Z70-Z76.Z73.3   Stress condition, not elsewhere classified

    Contraindications:

    Hypersensitivity, arterial hypertension, increased excitability, acute infectious diseases, myocardial infarction, arrhythmias, insomnia, cerebrovascular pathology; pregnancy, lactation; children's age (up to 12 years); reception without a break more than 90 days.

    Carefully:

    With a long course, stop taking the medication and take a break.

    Pregnancy and lactation:

    Category by FDA not determined. The drug is contraindicated in pregnancy and lactation.

    Dosing and Administration:

    Inside in the form of a liquid extract of 20-40 drops or in the form of tablets, 100-200 mg 2 times daily before meals. The course of treatment is 25-30 days; if necessary, repeat after 1-2 weeks.

    Side effects:

    Hypertension (high doses), agitation, insomnia, dizziness, anxiety, anxiety, excitement (high doses), nausea, vomiting, anorexia, increased levels of estrogen, increased vaginal bleeding, hypersensitivity reactions, rash.

    Overdose:

    Not described. Treatment is symptomatic.

    Interaction:

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

    Xanthine - increased excitability (not applied simultaneously).

    Kanamycin - increased toxic effects of kanamycin.

    Sugar reducing agents (chlorpropamide, glipizide, insulin soluble, metformin, tolazumide, tolbutamide) - increased hypoglycemia (not to be used in parallel).

    Cardiac glycosides (digoxin) - enhancement of the positive inotropic effect of glycosides (not applied simultaneously).

    Spruce European - an increase in the exciting and hypertensive effects (do not apply in parallel).

    Special instructions:

    Preference should be given to freshly prepared aqueous infusions from whole medicinal plant material.

    The drug is not recommended in the afternoon to avoid sleep disturbances.

    Instructions
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