Posted on 11/21/2021 6:47:13 PM PST by bitt
The Food and Drug Administration has provided its first batch of ‘confidential’ documents, in accordance with a FOIA lawsuit by the Public Health and Medical Professionals for Transparency. The redacted documents were the basis of the FDA’s Emergency Use Authorization of the Pfizer-BioNTech “vaccine*,” and subsequent federal vaccine mandates.
As reported earlier, the FDA does not intend to fully release the clinical trials information used to justify its authorization of the Pfizer-BioNTech ‘vaccine’ for 55 years. The non-partisan advocacy group’s sole mission is pressing for transparency in public health decision-making, such as the vaccine authorization process.
“The FDA has proposed to produce 500 pages per month which, based on its calculated number of pages, would mean it would complete its production in nearly 55 years – the year 2076,” the court filing said. “Until the entire body of documents provided by Pfizer to the FDA are made available, an appropriate analysis by the independent scientists that are members of Plaintiff is not possible.”
Two months after the lawsuit was filed, the FDA has produced the first 91 pages of the “more than 329,000 pages potentially responsive to Plaintiff’s FOIA request.” The findings, taken directly from the produced documents, are cited below.
“It is estimated that approximately [REDACTED] doses of BNT162b2 were shipped worldwide from the receipt of the first temporary authorisation for emergency supply on 01 December 2020 through 28 February 2021,” the document states.
“Cumulatively, through 28 February 2021, there was a total of 42,086 case reports (25,379 medically confirmed and 16,707 non-medically confirmed) containing 158,893 events,” the FDA document continues. “Most cases (34,762) were received from United States (13,739), United Kingdom (13,404) Italy (2,578), Germany (1913), France (1506), Portugal (866).”
Below is a General Overview of the reported outcomes to the Adverse Events:
(Excerpt) Read more at teamtuckercarlson.com ...
The redacted documents! Hey doc when do I get the results of my untimely death? oh in about 55 years
Phizer has some interesting things in its contracts, and had a full legal immunity put in.
True that ! A stall tactic taken right from the Dumbocratic party !
Then you add all the redacted information, and then you know that they have something to hide from the public.
When you factor in a surviveability rate of 98.4%, you really have to wonder what
and why they hide all the vaxxx information from the public.
They compel and mandate you to take an experimental shot "under emergency authorization " (UEA),
and then won't tell you how or why they arrived at that conclusion, and redact the data it generally means that
"there is something rotten in Denmark",.. and within the politicized FDA !
It is the same song & dance as Hillary’s emails.
I read another article about this, but I was at a restaurant and it would have been a pain to type a lengthy reply on my phone. So here goes.
This FDA resonse is highly insulting. In 1997, I was on a temp job in which our purpose was to label and copy thousands upon thousands of pages of documents, papers and so on related to a DOJ case. Our team of between 15 and 20 people (per 8-hour shift) must have been labeling, copying and lightly proofing thousands of pages a day. And there were usually 3 shifts a day — we were going 24 hours a day.
If the DOJ had been likewise furnishing only 500 pages a month, I would not have had an assignment. The FDA’s response is highly insulting. Maybe Rittenhouse can sue them along with all the people who defamed him.
Only a post turtle idiot strung out on CNN could accept such a scheme.
The FDA is the property of Big Pharma.
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