Clinical and pharmacological group: & nbsp

Anticoagulants

Included in the formulation
  • Cincumar
    pills inwards 
  • Included in the list (Order of the Government of the Russian Federation No. 2782-r of 30.12.2014):

    ONLS

    АТХ:

       

    B.01.A.A.07   Acenocoumarol

    Pharmacodynamics:Derivative of dihydrogenic acid. Prevents coagulation, disrupting synthesis in the liver of prothrombin II (prothrombin), VII (proconvertin), IX (Christmass), X (Stuart-Prower) - vitamin K-dependent factors of blood coagulation.
    Pharmacokinetics:

    After oral administration, it is absorbed in the digestive tract. The maximum concentration of the drug in the blood plasma is achieved after 3 hours. It binds to plasma proteins by 99%. When you re-receive cumulates. Passes through the placental barrier, enters the breast milk.

    Half-Elimination (half-life) of the drug is 8-9 hours. Metabolised in the liver. Elimination of 60% kidney, in the form of metabolites, 40% - with feces.

    The increase in prothrombin time and prothrombin index does not depend on the concentration of the drug in the blood plasma.

    Indications:

    It is used for thrombosis, thrombophlebitis, myocardial infarction, with the aim of preventing thromboembolic complications after surgical interventions.

    IX.I20-I25.I21   Acute myocardial infarction

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

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

    Contraindications:

    Hemorrhagic diathesis, renal and hepatic insufficiency, malignant neoplasms, hypoprothrombinemia (below 70%), hemorrhagic stroke, threatening miscarriage, peptic ulcer and duodenal ulcer, postpartum preeclampsia and eclampsia, pericarditis, post-lumbar puncture, organ biopsies.

    Individual intolerance.

    Carefully:

    Physical exhaustion, hypovitaminosis C. Women of childbearing age in a state where pregnancy is not excluded.

    Pregnancy and lactation:

    Pregnancy and lactation: recommendations for Food and Drug Administration (US Food and Drug Administration) - category C. In pregnancy and lactation, the use of the drug is contraindicated.

    Dosing and Administration:

    The dose of the drug depends on the initial indices of hemostasis. By the standard scheme is prescribed inside: the first day 6-8 mg per day, then up to 4 mg per day with prothrombin time in the range of 2-3.5 seconds. It is taken once a day at the same time.

    The highest daily dose: 16 mg.

    The highest single dose: 16 mg.

    Side effects:

    Central and peripheral nervous system: headache.

    Blood coagulation system: hemorrhages on the skin and mucous membranes, petechiae, post-traumatic hematomas, metrorrhagia, hemarthroses.

    Digestive system: dyspeptic disorders, diarrhea.

    Skin: alopecia, necrosis, "purple stop".

    Allergic reactions.

    Overdose:

    Hemorrhagic diathesis, epistaxis, bleeding gums, metrorrhagia, hematuria.

    Treatment: intravenous administration of 5-10 mg of phytomenadione (vitamin K), transfusion of freshly frozen blood plasma: 10-15 ml / kg of weight.

    Interaction:

    The effect of the drug is reduced when eating foods containing vitamin K: cauliflower, lettuce, liver, green peas, soy.

    Acenocoumarol enhances the effect of oral hypoglycemic drugs, ulcerogenic effects of glucocorticoids, toxic effects of phenytoin.

    Strengthen the effect of the drug some antibiotics: aminoglycosides, macrolides, tetracyclines, fluoroquinolones. The following preparations also increase the effect of acenocoumarol: cimetidine, tamoxifen, glucagon, non-steroidal anti-inflammatory drugs, metronidazole, methyldopa, pentoxifylline.

    Weaken the effects of acenocoumarol: barbiturates, oral contraceptives, ascorbic acid, antihistamines.

    Special instructions:

    Monitoring of hemostasis, control of general urine analysis.

    Patients receiving acenocoumarol, intramuscular injections should be avoided.

    The drug is withdrawn gradually, since there is a risk of thrombus formation.

    Instructions
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