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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
- Home Page - OpenVAERS
VAERS is the Vaccine Adverse Event Reporting System put in place in 1990 It is a voluntary reporting system that has been estimated to account for only 1% (read more about underreporting in VAERS) of vaccine injuries OpenVAERS is built from the HHS data available for download at vaers hhs gov
- 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
- VAERS Information - Health. mil
What is VAERS? The Vaccine Adverse Event Reporting System is a national vaccine safety surveillance program administered by the FDA and the CDC VAERS collects and analyzes information about adverse events that occur after the administration of U S licensed vaccines
- VAERS Fact Sheet--English
The Vaccine Adverse Event Reporting System (VAERS) is a national program managed by the U S Centers for Disease Control and Prevention (CDC) and the U S Food and Drug Administration (FDA) to monitor the safety of all vaccines licensed in the United States
- VAERS - Data
VAERS is one component of CDC's and FDA's multifaceted approach to monitoring safety after vaccines are licensed or authorized for use There are multiple, complementary systems that CDC and FDA use to capture and validate data from different sources
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