Covid-19 vaccines and VAERS

Posted on September 29th 2021 (over 3 years)

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Vaccine Adverse Event Reporting System, or VAERS, was created by the CDC and FDA to track vaccine safety. Healthcare providers and vaccine manufacturers are required by law to report adverse events. In addition, laypeople can report adverse events. Since the COVID-19 vaccines were initially issued under Emergency Use Authorization, VAERS rules expanded, and physicians had to report serious adverse events even if they did not think the vaccine caused the event. Dr. Seheult highlights how VAERS data can be misinterpreted as evidence that people are dying from the COVID-19 vaccine. As many people get vaccinated, the likelihood of some dying merely by chance increases. Moreover, most people being vaccinated early on were much older. In this clip, Dr. Roger Seheult explains how vaccine safety data is collected using the VAERS reporting system.

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