The Center for Biologics Evaluation and Research’s (CBER), Vaccines and Related Biological Products Advisory Committee (VRBPAC) met on October 22, 2020, and Slides and Video of the meeting are available for public viewing on the FDA Website.
The meeting revealed that the FDA knows that rushed-to-market COVID-19 vaccines may cause a wide range of life-threatening side effects, including death.
Unless the public is made aware of their real effects, and is given a choice, their widespread coercive promotion as “safe and effective” and “necessary” violates the medical ethical principle of informed consent.
Download Slides (Slide 16 Adverse Reactions)
Watch Adverse Reaction Discussion
www.fda.gov
UPDATE August 2021:
Please review the COVID Jab Adverse Event Reporting REAL LIFE Statistics from around the world. They demonstrate the serious adverse events that are taking place, including death from the COVID jabs.
Please also note that a 2010 study by the U.S. Department of Health and Human Services concluded that “fewer than 1% of vaccine injuries” are reported to VAERS (USA Adverse Event Data) and experts say the government’s reporting system is “broken.” Since Government reporting systems (in the USA, UK, Canada, Europe, Australia etc) are all voluntary systems, and Doctors have pressure not to report adverse events, when reading the Adverse Event Data keep in mind that this data could only represent 1% of actual adverse events.
Europe Adverse Event Data
