Peramivir
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| Trade names | Rapivab |
| AHFS/Drugs.com | Monograph |
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| Routes of administration | Intravenous |
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| Bioavailability | 100% (IV) |
| Elimination half-life | 7.7 to 20.8 hours (in patients with normal renal function) |
| Excretion | Kidney |
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| Formula | C15H28N4O4 |
| Molar mass | 328.413 g·mol−1 |
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| Influenza (flu) |
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Peramivir (trade name Rapivab) is an antiviral drug developed by BioCryst Pharmaceuticals for the treatment of influenza. Peramivir is a neuraminidase inhibitor, acting as a transition-state analogue inhibitor of influenza neuraminidase and thereby preventing new viruses from emerging from infected cells. It is approved for intravenous administration.[2]
In October 2009, the U.S. Food and Drug Administration (FDA) issued an emergency use authorization (EUA) for the use of peramivir based on safety data from phase I, phase II, and limited phase III trial data. The emergency use authorization for peramivir expired in June 2010.[3][4] On 19 December 2014, the FDA approved peramivir to treat influenza infection in adults.[2]
- ^ "The flu". Health Canada. 9 May 2018. Retrieved 13 April 2024.
- ^ a b Cite error: The named reference
FDA approvalwas invoked but never defined (see the help page). - ^ Thorlund K, Awad T, Boivin G, Thabane L (May 2011). "Systematic review of influenza resistance to the neuraminidase inhibitors". BMC Infectious Diseases. 11 (1): 134. doi:10.1186/1471-2334-11-134. PMC 3123567. PMID 21592407.
- ^ "Peramivir authorized for Emergency use". LifeHugger. 2009-12-04. Archived from the original on 2011-07-13. Retrieved 2009-12-04.