Published in Medical Letter on the CDC and FDA, September 24th, 2000
Robert P. Wise, MD, MPH, from the Center for Biologics Evaluation and Research, U.S. Food and Drug Administration (FDA), Rockville, Maryland, and colleagues analyzed adverse events reported to the U.S. Vaccine Adverse Event Reporting System (VAERS) from March 17, 1995, through July 25, 1998.
VAERS, jointly operated by the FDA and the Centers for Disease Control and Prevention (CDC), consolidates voluntarily submitted reports of...
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