Active Substance: Enoxaparin sodium.
Overview
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This medicine contains an important and useful components, as it consists of
Enoxaparin sodiumis available in the market in concentration
Enoxaparin Sodium
Renal or hepatic impairment, history of GI ulceration, uncontrolled hypertension, spinal or epidural anaesthesia; lactation and pregnancy; elderly. Periodic blood counts, platelet count and stool occult blood test recommended. Lactation: Excretion in milk unknown; not recommended
Myocardial infarction, Unstable angina, Venous thromboembolism, Deep vein thrombosis
Hypersensitivity, acute bacterial endocarditis; major bleeding disorder, haemorrhagic stroke, drug-induced thrombocytopenia.
1-10% Hemorrhage (1-4%),Elevation of serum aminotransferases (6%),Fever (5-8%),Local site reactions (2-5%),Thrombocytopenia (3%),Nausea (3%),Anemia (2%),Ecchymosis (3%) <1% Atrial fibrillation,Heart failure,Pulmonary edema,Pneumonia Potentially Fatal: Haemorrhagic complications.
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Enoxaparin is a low molecular weight heparin w/ anticoagulant properties. It acts by enhancing the inhibition rate of activated clotting factors including thrombin and factor Xa through its action on antithrombin III.
Increased risk of bleeding w/ anticoagulants, platelet aggregation inhibitors (e.g. dipyridamole, salicylates, NSAIDs, sulfinpyrazone). May increase bleeding w/ vit E.
Information not available