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

Updated: 2 days ago

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.


Three overloaded binders filled with numerous white paper documents.

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.



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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




Table 1: General Overview Selected Characteristics of All Cases (N=42886)

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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