The FDA has made public the first batch of documents it used to authorize Pfizer’s COVID shots, including a report detailing over 150,000 serious adverse events and more than 1,200 deaths connected to the jabs.
The data had been reviewed by the U.S. Food and Drug Administration (FDA) before it granted full approval to the Pfizer-BioNTech COVID-19 (BNT162b2) shots over the summer but had not been released to the public until last month.
- 31% of Pfizer recipients have died, or have long term or permanent side effects.
- Pregnant women who got Pfizer – 27% had serious events including miscarriages and still births.
- 38% of children who got Pfizer had an adverse event and did not get better.
READ THE PFIZER REPORT HERE: