The Vaccine Adverse Events Reporting system, referred to as VAERS, was a 1990 research project designed to detect potential problems with commonly administered inoculations not seen during pre-market testing, as well as ensure a stable supply of vaccines. The intention was to help medical researchers identify adverse bodily events related to vaccines, so if a trend emerged, they’d be able to monitor it.
This surveillance database, jointly managed by the CDC and the U.S. Food and Drug Administration (FDA), has become the subject of speculation and misinterpretation since the rollout of the COVID vaccine.
Turning Point USA founder Charlie Kirk recently speculated …
Send a tip to the news team at NR.
This article was originally published by Nationalreview.com. Read the original article here.