Clinical and pharmacological group: & nbsp

Fibrinolytics

Included in the formulation
  • Streptokinase
    lyophilizate in / in 
    BELMEDPREPARATY, RUP     Republic of Belarus
  • Thromboflue
    lyophilizate in / in 
  • Eber Biotech SA     Cuba
  • АТХ:

    B.01.A.D.   Enzyme preparations

    B.01.A.D.01   Streptokinase

    Pharmacodynamics:

    A highly purified protein preparation (enzyme), obtained from the culture of β-hemolytic streptococcus group C. When combined with profibrinolysin (plasminogen) forms a complex that activates its transition in the blood or blood clot into fibrinolysin (plasmin) - a proteolytic enzyme that dissolves fibrin fibers in blood clots and thrombi, causing degradation of fibrinogen and other plasma proteins, including coagulation factors V and VII. Dissolves thrombi, acting both on their surface and from the inside. Has antigenic properties.

    Pharmacokinetics:

    Introduced intravenously drip. The therapeutic effect develops 45 minutes after the start of the treatment. Biotransformation in the liver.

    The half-life period is 1 hour, the complex of stektokinase-plasminogen is 23 minutes. Pathways of excretion have not been studied.

    Indications:

    Introduced intravenously drip with thrombosis of deep, pulmonary embolism, acute myocardial infarction due to coronary thrombosis (in the first 3-6 hours), thrombosis of the vessels of the retina.

    VII.H30-H36.H34.8   Other retinal vascular occlusions

    IX.I20-I25.I21   Acute myocardial infarction

    IX.I26-I28.I26   Pulmonary embolism

    IX.I70-I79.I74   Embolism and thrombosis of the arteries

    IX.I80-I89.I82   Embolism and thrombosis of other veins

    Contraindications:

    Bleeding, hemorrhagic vasculitis, arterial hypertension (at systolic pressure over 200 mm Hg), within 3 months after a hemorrhagic stroke, acute pancreatitis, active form of tuberculosis, sepsis, individual intolerance.

    Carefully:

    Renal and hepatic insufficiency, the elderly age is over 75 years.

    Pregnancy and lactation:

    Recommendations for FDA - Category C. It is used for life indications after 18 weeks of pregnancy and during lactation.

    Dosing and Administration:

    Use in children

    1 month to 12 years 2500-4000 ME / kg intravenously drip for 30 minutes.

    Adults

    Intracoronary (intraarterially) to 20 thousand IU, followed by 2-4 thousand MI / min for 1 hour.

    Intravenous drip on 150 thousand IU for 1 hour.

    The highest daily dose: 180 thousand.

    The highest single dose: 80 thousand IU.

    Side effects:

    Blood coagulation system: hemorrhages in the peri-and myocardium, hematoma, bleeding at the injection sites, internal bleeding.

    Cardiovascular system: thromboembolism due to thrombus fragmentation.

    Reproductive system: violation of the menstrual cycle.

    Allergic reactions.

    Overdose:

    Massive hemorrhage.

    Treatment is symptomatic.

    Interaction:

    Simultaneous use with drugs that affect the blood clotting system (anticoagulants, heparin, antiaggregants) increases the risk of bleeding.

    Special instructions:

    Circulating antibodies to streptococci in the blood can inactivate streptokinase and reduce the effectiveness of treatment.

    The use of heparin after the administration of streptokinase is possible no earlier than 4 hours later.

    Instructions
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