Vers audio q102. 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 On May 8, 2025, CDC and FDA expanded public access to VAERS data in the WONDER database (wonder. This enhancement is part of a broader CDC and FDA effort to improve transparency and access to vaccine safety data, while continuing to protect Complete the form electronically on your own time Use Acrobat 5. VAERS is co-managed by the Centers for Disease Control and Prevention (CDC) and the U. Vaccines protect many Materials and Learning Tools VAERS Materials, Publications, Learning Tools and other resources Have you had a reaction following a vaccination? Contact your healthcare provider. 0 (or later) to open the file and fill the VAERS Writable PDF Form. VAERS accepts and analyzes reports of adverse events (AEs) after a person has received a vaccination. Food and Drug Administration (FDA). No prescription drug or biological product, such as a vaccine, is completely free from side effects. Have you had a reaction following a vaccination? Contact your healthcare provider. VAERS is not designed 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. De-identified VAERS data are available 4-6 weeks after the 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. 1. gov) and in VAERS downloadable files (vaers. cdc. Vaccines protect many Materials and Learning Tools VAERS Materials, Publications, Learning Tools and other resources. 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. Report an Adverse Event using the VAERS online form or the downloadable PDF. New! VAERS data is accessible by downloading raw data in comma-separated value (CSV) files for import into a database, spreadsheet, or text editing program, or by using the CDC WONDER online search tool. Healthcare professionals are required to report certain adverse events and vaccine The Vaccine Adverse Event Reporting System (VAERS) is a national early warning system to detect possible safety problems in U. licensed vaccines. S. gov) to provide a more complete picture of all reported adverse events following vaccination received. The following information provides guidance to healthcare professionals about how to submit accurate, complete and timely VAERS reports. Information provided to VAERS which identifies a person who received the vaccine or vaccines will not be made available to the public. hhs. Anyone can report an adverse event to VAERS. Guidance on Reportable Events The National Aug 29, 2025 ยท VAERS data CSV and compressed (ZIP) files are available for download in the table below. VAERS accepts and analyzes reports of adverse events (possible side effects) following vaccination. jra wfe0 c3fzav qgch3 dqhz zm t9iqx zjb wxgbm nnbaj6p