Clinical and pharmacological group: & nbsp

Antihypoxants and antioxidants

Regenerants and reparants

Included in the formulation
  • Actovegin®
    solution d / infusion 
  • Actovegin®
    solution for injections 
  • Actovegin
    solution for injections 
    Nycomed Austria GmbH     Austria
  • Actovegin
    pills inwards 
  • Actovegin®
    solution d / infusion 
    Nycomed Austria GmbH     Austria
  • Actovegin®
    ointment externally 
  • Actovegin®
    gel externally 
  • Actovegin®
    cream externally 
  • Solcoseryl
    ointment externally 
  • Solcoseryl
    gel externally 
  • Solcoseryl
    solution w / m in / in 
  • Solcoseryl
    gel d / eye 
  • АТХ:

    B.06.A.B   Other hematological preparations

    Pharmacodynamics:

    Hemoderivat obtained by dialysis and ultrafiltration contains substances with molecular weight less than 5000 Daltons (Ya). Accelerates the processes of utilization of oxygen and glucose at the molecular level.Strengthening the energy metabolism, ensures the stability of cells to hypoxia in conditions of ischemia. It normalizes pH, accelerates blood circulation, decomposition of beta-hydroxybutyrate and lactate, improves tissue trophism.

    Pharmacokinetics:

    After parenteral administration, the therapeutic effect develops after 30 minutes and lasts for 3 hours.

    Indications:

    It is used to treat metabolic and circulatory disorders of the central nervous system: with ischemic stroke, craniocerebral trauma, encephalopathy of various genesis. It is used for violations of peripheral arterial and venous circulation, angiopathy, including diabetes mellitus. Used to regenerate tissues for ulcers, bedsores, burns, radiation damage to the skin and mucous membranes. It is used to treat radiation neuropathy.

    IX.I20-I25.I25.2   Postponed myocardial infarction

    IX.I60-I69.I63   Cerebral infarction

    IX.I60-I69.I67.9   Cerebrovascular disease, unspecified

    IX.I60-I69.I69   Effects of cerebrovascular disease

    IX.I70-I79.I73.9   Peripheral vascular disease, unspecified

    IX.I70-I79.I79.2 *   Peripheral angiopathy in diseases classified elsewhere

    IX.I80-I89.I87.2   Venous insufficiency (chronic) (peripheral)

    IX.I95-I99.I99   Other and unspecified disorders of the circulatory system

    XII.L55-L59.L58   Radiation dermatitis radiation

    XII.L80-L99.L89   Decubital ulcer

    XIV.N30-N39.N30.4   Radiation cystitis

    XIX.S00-S09.S06   Intracranial injury

    XIX.T08-T14.T14.1   Open wound of unspecified area of ​​the body

    XIX.T20-T32.T30   Thermal and chemical burns, unspecified

    XIX.T79.T79.3   Post-traumatic wound infection, not elsewhere classified

    VI.G60-G64.G63.2 *   Diabetic polyneuropathy (E10-E14 + with common fourth sign .4)

    Contraindications:

    Severe cardiovascular failure, oliguria, anuria, pulmonary edema, fluid retention in the body, individual intolerance.

    Carefully:

    Pregnancy and lactation, hypernatremia, hyperchloremia, hypersensitivity.

    Pregnancy and lactation:

    Recommendations for FDA - Category B. Applicable with caution, in cases where the expected effect exceeds the risk to the fetus and newborn.

    Dosing and Administration:

    Use in children

    Intramuscularly or intravenously:

    newborns and children under 3 years of age - 0.4-0.5 ml / kg once a day;

    3-6 years - 0.25-0.4 mg / kg once a day.

    Adults

    Intravenous drip or jet, intraarterially - 5-20 ml per day. Intramuscularly, slowly - no more than 5 ml per day.

    The highest daily dose: 2 g of dry matter per 250 ml of 5% solution dextrose or 0.9% sodium chloride.

    Side effects:

    Allergic reactions.

    Overdose:

    Cases of overdose are not described.

    Treatment is symptomatic.

    Interaction:

    Clinically significant interactions are not described.

    Special instructions:

    The drug is on the anti-doping control list.

    Instructions
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