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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)
- 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 - 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
- Vaccine Adverse Events | FDA
VAERS collects and analyzes information from reports of adverse events (possible side effects) that occur after the administration of US licensed vaccines
- 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
- VAERS - Data
VAERS accepts reports of adverse events that occur following vaccination Anyone, including Healthcare providers, vaccine manufacturers, and the public can submit reports to the system
- Vaccine Adverse Event Reporting System (VAERS) Questions and Answers
VAERS collects and analyzes data from reports of adverse events following vaccination Since 1990, VAERS has received over 2 million reports, most of which describe mild side effects such as
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