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January 8, 2021 (LifeSiteNews) – The list of people who have visited emergency rooms after receiving a COVID-19 vaccine is in the hundreds and those who have suffered adverse reactions is over 1,000, according to the Vaccine Adverse Event Reporting System (VAERS).
VAERS is a system of reporting managed by the Centers for Disease Control and Prevention (CDC) and the Federal Drug Administration (FDA). It collects information from the public regarding bad reactions to vaccines. The CDC and FDA find the data useful for detecting any potential problems early on with U.S.-licensed vaccines. According to its website, “Healthcare professionals are required to report certain adverse events and vaccine manufacturers are required to report all adverse events that come to their attention.”
Since the earliest days of the first injections administered, people started experiencing things like “nausea, tremors, stabbing pain, and wheezing.”
“A healthcare worker at Bartlett Regional Hospital in Alaska suffered a suspected severe allergic reaction, or anaphylaxis, after receiving Pfizer’s vaccine. She was taken to the emergency room and spent several nights there before being discharged,” reported The Epoch Times.
Since then, a second health care worker
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