FDA Adverse Event Reporting System (FAERS) Database
FDA Adverse Event Reporting System Database supports the FDA's post-marketing safety surveillance program for all marketed drug and therapeutic biologic products.
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 …
Vaccine Adverse Event Reporting System (VAERS)
Have you had a reaction following a vaccination? Contact your healthcare provider. Report an Adverse Event using the VAERS online form or the downloadable PDF. New!
FDA Adverse Event Reporting System (FAERS) Essentials: A …
May 19, 2025 · Postmarketing safety surveillance promotes the identification of adverse events not known at the time of approval. Adverse event reports, also called individual case safety …
FDA Adverse Event Reporting System - Wikipedia
The FDA Adverse Event Reporting System (FAERS or AERS) is a computerized information database designed to support the U.S. Food and Drug Administration 's (FDA) postmarketing …
Questions and Answers on FDA's Adverse Event Reporting System …
This Question and Answers about FDA’s database that contains information on adverse event and medication error reports submitted to FDA.
Submitting a Vaccine Adverse Event Reporting System (VAERS) Report …
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 - 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 …
FDA Adverse Event Reporting System
The FDA Adverse Event Reporting System (FAERS) is a database that contains information on adverse event and medication error reports submitted to FDA. The database is designed to …
FDA Begins Real-Time Reporting of Adverse Event Data
Aug 22, 2025 · FAERS is the FDA's primary database for collecting and analyzing adverse event reports, serious medication errors, and product quality complaints for prescription drugs and …