Identifying patterns of adverse event reporting for four members of the angiotensin II receptor blockers class of drugs: revisiting the Weber effect
Author:
Publisher
Wiley
Subject
Pharmacology (medical),Epidemiology
Reference10 articles.
1. Title 21 of the Code of Federal Regulations, Subpart 314.80. Additionally, 21 CFR 310.305 and 21 CFR 314.98.
2. Temporal patterns of NSAID spontaneous adverse event reports: the Weber effect revisited;Wallenstein;Drug Saf,2001
3. Replication of the Weber effect using postmarketing adverse event reports voluntarily submitted to the United States Food and Drug Administration;Hartnell;Pharmacotherapy,2004
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