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Title
Adverse drug event surveillance and drug withdrawals in the United States, 1969-2002: the importance of reporting suspected reactions.
Authors
Wysowski, Diane K; Swartz, Lynette
Abstract
The Adverse Event Reporting System is the primary surveillance database used by the Food and Drug Administration for identifying postmarketing drug safety problems.
Publication
Archives of internal medicine, 2005, Vol 165, Issue 12, p1363