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  • 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!
  • 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 more information for 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 patient
  • 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 - Resources
    Materials and Learning Tools VAERS Materials, Publications, Learning Tools and other resources
  • 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
  • VAERS - Download Upload a Writable PDF Form
    Complete the form electronically on your own time Use Acrobat 5 0 (or later) to open the file and fill the VAERS Writable PDF Form
  • 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 Data Use Guide
    1 Important Information About VAERS The Vaccine Adverse Event Reporting System (VAERS) was created by the Food and Drug Administration (FDA) and Centers for Disease Control and Prevention (CDC) to receive reports about adverse events that may be associated with vaccines No prescription drug or biological product, such as a vaccine, is completely free from side effects Vaccines protect many
  • Guide to Interpreting VAERS Data - HHS. gov
    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* Vaccine Toxoid . . .
    **Represents the onset interval between vaccination and the adverse event For a detailed explanation of terms, see the Vaccine Injury Table at





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