Zanamivir: Difference between revisions

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'''| [[Zanamivir clinical studies|Clinical Studies]]'''
'''| [[Zanamivir clinical studies|Clinical Studies]]'''
'''| [[Zanamivir dosage and administration|Dosage and Administration]]'''
'''| [[Zanamivir dosage and administration|Dosage and Administration]]'''
'''| [[Zanamivir compatibility reconstitution and stability|Compatibility, Reconstitution, and Stability]]'''
'''| [[Zanamivir directions for use|Directions For Use]]'''
'''| [[Zanamivir directions for use|Directions For Use]]'''
'''| [[Zanamivir how supplied|How Supplied]]'''
'''| [[Zanamivir how supplied|How Supplied]]'''

Revision as of 21:06, 29 December 2013

Zanamivir
RELENZA® FDA Package Insert
Description
Clinical Pharmacology
Microbiology
Indications and Usage
Contraindications
Warnings and Precautions
Adverse Reactions
Overdosage
Clinical Studies
Dosage and Administration
Directions for Use
How Supplied
Labels and Packages

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Zanamivir (INN) (IPA: Template:IPA) is a neuraminidase inhibitor used in the treatment of and prophylaxis of both Influenzavirus A and Influenzavirus B. Zanamivir was the first neuraminidase inhibitor commercially developed. It is currently marketed by GlaxoSmithKline under the trade name Relenza. Relenza is the only type of Zanamivir.

Category

Antiviral

US Brand Names

RELENZA®

FDA Package Insert

Description | Clinical Pharmacology | Microbiology | Indications and Usage | Contraindications | Warnings and Precautions | Adverse Reactions | Overdosage | Clinical Studies | Dosage and Administration | Directions For Use | How Supplied | Labels and Packages

Mechanism of Action

Zanamivir is an inhibitor of influenza virus neuraminidase affecting release of viral particles.

References