Home » Anti-Vaccine Propaganda » Using and Misusing VAERS Reports

Using and Misusing VAERS Reports

The Vaccine Adverse Event Reporting System (VAERS) is considered “an early warning system to detect possible safety issues with U.S. vaccines.”

Created as part of the National Childhood Vaccine Injury Act in 1990, anyone can report possible vaccine reactions to VAERS.

Using and Misusing VAERS Reports

Just remember that just because something is reported to VAERS and is included in the VAERS database, that doesn’t automatically mean that a vaccine caused the reaction.

Additional information is sometimes requested to further look into these reactions, including medical records.

“Reports of all possible associations between vaccines and adverse events (possible side effects) are filed in VAERS. Therefore, VAERS collects data on any adverse event following vaccination, be it coincidental or truly caused by a vaccine. The report of an adverse event to VAERS is not documentation that a vaccine caused the event.”

Guide to Interpreting VAERS Data

For example, one study of VAERS reports found that only 3% of the adverse events following immunization “were classified as definitely causally related to vaccine received.”

Despite its limitations, VAERS works well.

It was using VAERS data that CDC and FDA vaccine experts quickly discovered that the older RotaShield rotavirus vaccine was associated with an increased risk of intussusception.

More on Misusing VAERS Reports

Last Updated on April 6, 2024

Discover more from VAXOPEDIA

Subscribe now to keep reading and get access to the full archive.

Continue reading