Noxarin 6000 Anti-Xa IU/0.6 ml (SC Injection)
Medicine Details
Category | Details |
---|---|
Generic | Enoxaparin sodium |
Company | Opsonin pharma ltd |
Also available as |
Indications
- Treatment of deep vein thrombosis, with or without pulmonary embolism
- Treatment of unstable angina and non-Q-wave myocardial infarction
- Prevention of thrombus formation in the extra-corporal circulation during haemodialysis
- Prophylaxis of venous thromboembolic disease in surgical and medical patients
Composition
- Enoxaparin Sodium BP 20 mg equivalent to 2000 anti-Xa III
- Enoxaparin Sodium BP 40 mg equivalent to 4000 anti-Xa III
- Enoxaparin Sodium BP 60 mg equivalent to 6000 anti-Xa IU
- Enoxaparin Sodium BP 80 mg equivalent to 8000 anti-Xa IU
Pharmacology
Low molecular weight heparin with high anti-Xa activity and low anti-lla or antithrombin activity. Metabolised in the liver.
Dosage
- Deep vein thrombosis:
- Subcutaneously 100 anti-Xa IU/kg twice daily for 10 days
- Subcutaneously 150 anti-Xa IU/kg once daily for 10 days
- Unstable angina and non-Q-wave myocardial infarction: Subcutaneously 100 anti-Xa IU/kg twice daily for 2-8 days
- Prevention of thrombus formation during hemodialysis: Recommended dose is 100 anti-Xa IU/kg
- Venous thromboembolic disease in surgical patients:
- Subcutaneously 2000 anti-Xa IU once daily for 7-10 days
- Subcutaneously 4000 anti-Xa IU once daily for 7-10 days
- Subcutaneously 4000 anti-Xa IU once daily for 3 weeks following initial therapy
- Venous thromboembolic disease in medical patients: Subcutaneously 4000 anti-Xa IU once daily for 6-14 days
Administration
Instructions on self-administration including injection site preparation, selecting the dose, and injecting process
Interaction
Recommends discontinuation of agents affecting hemostasis prior to Noxarin therapy unless strictly indicated
Contraindications
Hypersensitivity to Enoxaparin Sodium, active major bleeding, and high risk of uncontrolled hemorrhage including recent hemorrhagic stroke
Side Effects
- Haemorrhage (bleeding)
- Thrombocytopenia
- Skin rash at injection sites
- Neuraxial hematomas with concurrent use of Noxarin and spinal/epidural anesthesia
Pregnancy & Lactation
Pregnancy category B. No evidence of crossing the placental barrier. Use during pregnancy only if clearly needed. Consideration for nursing mothers
Precautions & Warnings
Deep subcutaneous route administration, caution in conditions with increased potential for bleeding, platelet count measurement recommended
Use in Special Populations
- No dose adjustment in elderly patients unless kidney function is impaired
- Careful observation for signs and symptoms of bleeding in renal impairment patients
- Caution in hepatically impaired patients
Overdose Effects
Hemorrhagic complications, neutralization by slow i.v. injection of protamine sulfate
Therapeutic Class
Parenteral anti-coagulants
Storage Conditions
Store in a cool and dry place, protect from light and moisture, do not store above 25°C, keep out of the reach of children
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