As part of the National Childhood Vaccine Injury Act of 1986 (NCVIA), health professionals and vaccine manufacturers are able to report adverse events that occur following a routine vaccine injection. In response, the Center for Disease Control and Prevention (CDC) and the Food and Drug Administration (FDA) created the Vaccine Adverse Event Reporting System (VAERS) in 1990 as a means for tracking this information. Learn more about the VAERS program:
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