FDA Pfizer Report: 1223 Deaths & 150,000+ Serious Adverse events occurred in the first 3 months

Breaking News: The FDA has released the first set of documents used to approve Pfizer's COVID vaccines, including a report detailing over 150,000 serious adverse events and over 1,200 deaths linked to the vaccines.



The data was reviewed by the US Food and Drug Administration (FDA) before the Pfizer-BioNTech COVID-19 (BNT162b2) shots were given full approval over the summer, but it wasn't made public until last month.

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Pfizer recipients have died in 31% of cases, or have long-term or permanent side effects.

Pregnant women who took Pfizer had a 27 percent chance of having serious complications, such as miscarriages and stillbirths.

Pfizer caused an adverse event in 38% of children who received it, and they did not get better.


Below is a copy of the FDA Report that admits there have been


5.3.6-postmarketing-experience
.pdf
Download PDF • 1.01MB


Note there have been 1223 Fatalities form this one drug company alone in the first 3 months of being in circulation for experimental use with 9400 unknown.



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