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- Vaccine Adverse Event Reporting System (VAERS)
Report an Adverse Event using the VAERS online form or the downloadable PDF New! Important: If you are experiencing a medical emergency, seek immediate assistance from a healthcare provider or call 9-1-1
- Vaccine Adverse Event Reporting System (VAERS) Questions and Answers
VAERS is a national vaccine safety surveillance program created as an outgrowth of the National Childhood Vaccine Injury Act of 1986 (NCVIA) and is administered by the Food and Drug
- About the Vaccine Adverse Event Reporting System (VAERS)
On May 8, 2025, CDC and FDA expanded public access to VAERS data in the WONDER database (wonder cdc gov) and in VAERS downloadable files (vaers hhs gov) to provide a more complete picture of all reported adverse events following vaccination received
- Vaccine Adverse Event Reporting System - Wikipedia
VAERS is a postmarketing surveillance program, collecting information about adverse events (possible harmful side effects) that occur after administration of vaccines to ascertain whether the risk–benefit ratio is high enough to justify continued use of any particular vaccine
- VAERS - Report an Adverse Event - HHS. gov
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
- What Is VAERS and How Does It Help Vaccine Safety? - WebMD
The Vaccine Adverse Event Reporting System (VAERS) helps the CDC and FDA spot possible safety problems with vaccines licensed in the U S Learn more about how it works
- What VAERS Is (And Isn’t) - Johns Hopkins
VAERS is a publicly available, searchable database of reports that have not been verified It simply contains whatever people have voluntarily reported Moreover, the CDC and FDA do not restrict what people can report, as long as it happened at some point following a vaccination
- VAERS Overview | FDA - U. S. Food and Drug Administration
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)
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