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- Vaccine Adverse Event Reporting System (VAERS)
VAERS is co-sponsored by the Centers for Disease Control and Prevention (CDC), and the Food and Drug Administration (FDA), agencies of the U S Department of Health and Human Services (HHS)
- VAERS Overview | FDA
The Vaccine Adverse Event Reporting System (VAERS) is a valuable tool for post-marketing safety surveillance (monitoring after a product has been approved and is on the market)
- About the Vaccine Adverse Event Reporting System (VAERS)
The Vaccine Adverse Event Reporting System (VAERS) is the nation's early warning system that monitors the safety of FDA-approved vaccines and vaccines authorized for use for public health emergencies
- What Is VAERS and How Does It Monitor Vaccine Safety? | mctlaw
VAERS is a national reporting system used to monitor vaccine safety by collecting and analyzing reports of adverse events following vaccination
- Search Vaccine Lots - OpenVAERS
VAERS accepts reports of adverse events and reactions that occur following vaccination Healthcare providers, vaccine manufacturers, and the public can submit reports to the system While very important in monitoring vaccine safety, VAERS reports alone cannot be used to determine if a vaccine caused or contributed to an adverse event or illness
- What to know about VAERS | Vaccine Resource Hub
This four-slide carousel explains the Vaccine Adverse Event Reporting System (VAERS), emphasizes how the anti-vaccine movement misuses VAERS data, and highlights how scientists use VAERS as part of broader vaccine monitoring
- Vaccine Adverse Events: VAERS Reporting and VICP Claims
Learn how to report vaccine adverse events through VAERS and what to expect if you pursue a compensation claim through the VICP or CICP
- VAERS - Report an Adverse Event
The Vaccine Adverse Event Reporting System (VAERS) is a national early warning system to detect possible safety problems in vaccines used in the United States VAERS accepts and analyzes reports of adverse events (AEs) after a person has received a vaccination
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