VAERS reports
VAERS reports
The Vaccine Adverse Event Reporting System (VAERS) is a cooperative program for vaccine safety of the Centers for Disease Control and Prevention (CDC) and the U.S. Food and Drug Administration (FDA). VAERS allows coordinated and centralized monitoring of possible adverse events (possible side effects) that occur after the administration of U.S.-licensed vaccines.
Health professionals are required to report all reactions that occur after a vaccination, regardless of whether symptoms seem more likely to be related to another condition or illness. Anyone can submit a report.
Just because a reaction was reported to VAERS does not mean the vaccine caused the reaction. Careful studies are conducted if a pattern emerges that suggests potential problems with a vaccine.
Current as of: October 24, 2023
Author: Healthwise Staff
Clinical Review Board
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This information does not replace the advice of a doctor. Healthwise, Incorporated, disclaims any warranty or liability for your use of this information. Your use of this information means that you agree to the Terms of Use. Learn how we develop our content.