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9.3.5.7: The Vaccine Adverse Event Reporting System (VAERS)

  • Page ID
    90385
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    The Vaccine Adverse Event Reporting System ( VAERS) is a national vaccine safety surveillance program for reporting adverse events after administering any vaccine in the United States. VAERS is co-managed by the Centers for Disease Control and Prevention (CDC) and the U.S. Food and Drug Administration (FDA). Anyone can report an adverse event to VAERS, but healthcare professionals must report certain adverse events, and vaccine manufacturers must report all adverse events that come to their attention. Adverse events should be reported even if the cause of the adverse event is uncertain (U.S. Department of Health and Human Services, n.d.)


    This page titled 9.3.5.7: The Vaccine Adverse Event Reporting System (VAERS) is shared under a CC BY 4.0 license and was authored, remixed, and/or curated by Anna Jannak (Consortium of Academic and Research Libraries in Illinois (CARLI)) .

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