From Mdwiki ![]() | |
| Names | |
|---|---|
| Trade names | Fraxiparin(e), Fraxodi, others |
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| Clinical data | |
| Routes of use | Subcutaneous injection (except for haemodialysis) |
| External links | |
| AHFS/Drugs.com | International Drug Names |
| Legal | |
| Legal status | |
| Pharmacokinetics | |
| Bioavailability | 89% (SC dose) |
| Elimination half-life | 3.7 hours (SC dose) |
| Excretion | clearance 21.4mL/min (+/- 7) |
| Chemical and physical data | |
| Molar mass | 4300 g/mol |
Nadroparin (trade names Fraxiparin[e], Fraxodi, among others) is an anticoagulant used in general and orthopedic surgery to prevent thromboembolic disorders (deep vein thrombosis and pulmonary embolism), and as treatment for deep vein thrombosis. It is also used to prevent clotting during hemodialysis, and for treatment of unstable angina and non-Q wave myocardial infarction.[1] It is given by injection under the skin.
It is in the low molecular weight heparin (LMWH) class.
It is on the World Health Organization's List of Essential Medicines as an alternative to enoxaparin.[2]
Nadroparin was developed by Sanofi-Synthélabo.
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Categories: [Heparins] [World Health Organization essential medicines (alternatives)]
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