FDA Releases Month One Of 55 Year Rollout For Pfizer COVID-19 Jab Data And It’s Already A Disaster

More from Pfizer!

Remember the request regarding the release of data and information for Pfizer jabs. Well, here’s more from the FOIA request:

In the United States District Court for the Northern District of Texas, Public Health and Medical Professionals for Transparency had a “FOIA” request for data and information of Pfizer’s coronavirus vaccine.

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The FDA requested a slower rate of processing the information obtained from Pfizer. That’s 329,000+ pages! The FDA suggested a processing rate of 500 pages per month, meaning they need 658 months or 55 years.

From the Second Joint Report:

After the December 1 production, FDA proposes to work through the list of documents that Plaintiff requested FDA prioritize for production in order of priority and process and release the non-exempt portions of those records to Plaintiff on a rolling basis. FDA proposes to process and produce the non-exempt portions of responsive records at a rate of 500 pages per month. This rate is consistent with processing schedules entered by courts across the country in FOIA cases.3 Plaintiff’s request (as set forth below) that FDA process and produce the non-exempt portions of more than 329,000 pages in four months would force FDA to process more than 80,000 pages per month. Undersigned counsel is not aware of any court ever granting such a request. The Court should decline to enter Plaintiff’s schedule for numerous reasons.

On Friday, the FDA offered the first 91+ pages of the documentation.

Aaron Siri had the details in Injecting Freedom:

Pfizer explains, on page 6, that “Due to the large numbers of spontaneous adverse event reports received for the product, [Pfizer] has prioritised the processing of serious cases…” and that Pfizer “has also taken a [sic] multiple actions to help alleviate the large increase of adverse event reports” including “increasing the number of data entry and case processing colleagues” and “has onboarded approximately [REDACTED] additional fulltime employees (FTEs).”  Query why it is proprietary to share how many people Pfizer had to hire to track all of the adverse events being reported shortly after launching its product.

As for the volume of reports, in the 2 ½ months following EUA, Pfizer received a total of 42,086 reports containing 158,893 “events.”  Most of these reports were from the U.S. and disproportionately involved women (29,914 vs. 9,182 provided by men) and those between 31 and 50 years old (13,886 vs 21,325 for all other age groups combined, with another 6,876 whose ages were unknown).  Also, 25,957 of the events were classified as “Nervous system disorders”

In the first 75 days of the coronavirus vaccine rollout following EUA, Pfizer hired more people to track adverse events.

Nervous system disorders?

Imagine the outcome of the process!

Click here to check out the documents.

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Source: WeLoveTrump

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