Adefovir: Difference between revisions

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

Revision as of 00:49, 2 January 2014

Adefovir
HEPSERA® FDA Package Insert
Description
Clinical Pharmacology
Microbiology
Indications and Usage
Contraindications
Warnings and Precautions
Adverse Reactions
Overdosage
Clinical Studies
Dosage and Administration
How Supplied
Labels and Packages

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

Overview

Adefovir dipivoxil, previously called bis-POM PMEA, with trade names Preveon® and Hepsera®, is an orally-administered nucleotide analog reverse transcriptase inhibitor (ntRTI) used for treatment of hepatitis B. It is a failed treatment for HIV.

Category

Antiviral

US Brand Names

HEPSERA®

FDA Package Insert

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

Mechanism of Action

References