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Vaccine Adverse Event Reporting System (VAERS) Important: If you are experiencing a medical emergency, seek immediate assistance from a healthcare provider or call 9-1-1 CDC and FDA do not provide individual medical treatment, advice, or diagnosis If you need individual medical or health care advice, consult a qualified healthcare provider
VAERS - Data 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 This enhancement is part of a broader CDC and FDA effort to improve transparency and access to vaccine safety data, while continuing to protect
VAERS - About Us Background and Public Health Importance Established in 1990, the Vaccine Adverse Event Reporting System (VAERS) is a national early warning system to detect possible safety problems in U S -licensed vaccines VAERS is co-managed by the Centers for Disease Control and Prevention (CDC) and the U S Food and Drug Administration (FDA) VAERS accepts and analyzes reports of adverse events (possible
VAERS - Information for Healthcare Providers Home Resources Information for Healthcare Providers En Español Information for Healthcare Providers Safety monitoring in VAERS relies on receiving reports of vaccine adverse events from healthcare professionals The following information provides guidance to healthcare professionals about how to submit accurate, complete and timely VAERS reports Guidance on Reportable Events The National
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 Anyone can report an adverse event to VAERS Healthcare professionals are required to report certain adverse events and vaccine
VAERS - Data Sets VAERS data CSV and compressed (ZIP) files are available for download in the table below For information about VAERS data, please view the VAERS Data Use Guide [PDF - 310KB], which contains the following information: Important information about VAERS from the FDA Brief description of VAERS Cautions on interpreting VAERS data Definitions of terms Description of files List of commonly used
VAERS - FAQs VAERS collects national data from all U S states and territories The VAERS form collects information about the vaccine, the person vaccinated and the adverse event VAERS can be used as an early warning system to identify rare adverse events VAERS is a tool for identifying potential vaccine safety concerns that need further study using more robust data systems It is generally not possible to
Guide to Interpreting VAERS Data 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 This enhancement is part of a broader CDC and FDA effort to improve transparency and access to vaccine safety data, while continuing to protect
VAERS Table of Reportable Events Following Vaccination Events described in manufacturer’s package insert as contraindications to additional doses of vaccine (interval - see package insert) Effective date: January 8, 2024 The Reportable Events Table (RET) reflects what is reportable by law (42
VAERS - Resources VAERS will undergo routine maintenance on the third Thursday of each month from 8:30 p m EST until Friday at 12:30 a m EST VAERS will undergo Network maintenance on 12 06 2025 from 8:30 a m to 12:30 p m EST The website and data access services will be unavailable during this time Please contact us at support@VAERS org if you have any questions