1200 deaths KNOWN in 90 days by Phizer...FOIA docs releases... its underreported too

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The Food and Drug Administration (FDA) released the first batch of documents related to Pfizer’s Covid-19 vaccine after a federal judge ordered that they must comply with a massive Freedom of Information Act (FOIA) request that was filed by a government accountability group called Public Health and Medical Professionals for Transparency.

The esteemed group of more than 30 professors and scientists asked the federal government to share any and all data that factored into the agency’s hasty decision to grant Pfizer’s experimental mRNA vaccine an emergency use authorization (EUA) – which amounts to a trove of over 329,000 documents.



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The FDA challenged the FOIA request in court. After the agency was told that it must turn over the documents, Justice Department lawyers representing the FDA asked a federal judge to allow them an unthinkable 55 years to process the request, saying that they would be able to release just 500 pages a month.

A motion that was also filed by the same group of doctors and scientists is currently pending in federal court that would force the FDA to expedite processing and releasing these documents.



Meanwhile, the FDA still has to comply with the original order to begin turning over documents.


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According to an official Pfizer document that is titled Cumulative Analysis of Post-Authorization Adverse Event Records Reports, in just the first 90 days of the vaccine’s roll out under the FDA’s EUA – from December 1st. 2020 – February 28th, 2021 – there were TENS OF THOUSANDS of reported adverse reactions, including OVER 1200 DEATHS.



The document also makes it clear that the data only includes “recorded adverse events,” which even the author admits is likely just a portion of the true number of adverse reactions that took place.

Again, keep in mind, this is within the first 90 days of the Pfizer jab’s availability.


From the Pfizer document:
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“Reports are submitted voluntarily, and the magnitude of underreporting is unknown.

Some of the factors that may influence whether an event is reported include: length of time since marketing, market share of the drug, publicity about a drug or an AE, seriousness of the reaction, regulatory actions, awareness by health professionals and consumers of adverse drug event reporting, and litigation.”




Oh yes you knew. The VAERS system is pretty clear.



LINK

A PDF of the documents are in the link.


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Pfizer’s “confidential” Covid-19 vaccine adverse reaction review ends with thousands of conditions that are of “special interest” and could possibly develop after taking their experimental jab. The single-space typed list continues for an astonishing 9 pages.