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 …
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)
Aug 7, 2024 · 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 …
How a Federal Vaccine Safety Database Became a Magnet for ...
Dec 22, 2025 · The Vaccine Adverse Event Reporting System (VAERS) was established to protect public health. Now it's being used against it.
Jan 16, 2025 · VAERS is a monitoring system for reported adverse events following vaccination jointly operated by FDA and the Centers for Disease Control and Prevention (CDC). An …
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 …
VAERS Overview | FDA
Aug 12, 2021 · 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 …
Interview: How the U.S. Government Monitors Vaccine Safety
Dec 19, 2025 · The database, the Vaccine Adverse Event Reporting System, known as VAERS, serves as a repository to which people can voluntarily report health problems that occur after …
Submitting a Vaccine Adverse Event Reporting System (VAERS) …
May 9, 2025 · Submitting reports of adverse events (any side effect or health problem after vaccination that is concerning to you, even if you are not sure if the vaccine caused the event) …
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.