The headline maybe looks like clickbait, but it’s accurate that the FDA asked for permission from a federal judge.
The federal agency wants to withhold the disclosure of the data and information of the C-19 shot for 55 years.
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We know that Pfizer needs a further investigation and a larger sample size to find if their vaccines are suitable for children with the available documents.
The latest discoveries say that Pfizer hid the accurate numbers of trial deaths after getting the vaccine. The real number of deaths was 21.
Alex Berenson reported: The one-paragraph summary: Pfizer told the world 15 recipients of Comirnaty had died in its pivotal trial. The real number was 21 – compared to only 17 people who didn’t get the shot.
URGENT: Alex Berenson wants to get this out. Please consider retweeting. What do I think? I believe this vaccine is worse than a dud. Millions will die.https://t.co/y7O7SN9Ioq
— Mahound's Paradise (@MahoundParadise) November 17, 2021
There is evidence that Pfizer and the FDA don’t want to disclose before the rollout of the vaccines to millions of people. VAERS database of CDC website stated that there were 2.3 million side effects only from the Pfizer shot.
What else will come up until 2076?
The USA district court for the Northern District of Texas, Public Health and Medical Professionals for Transparency, issued a FOIA request for disclosure of data of the Pfizer vaccine.
They wanted the FDA to provide the non-exempt portions of the data in 4 months. However, the FDA asked for a slower rate of processing the 329,000 and more pages of data that Pfizer shared. The FDA proposed a processing rate of 500 pages for a month.
Second Joint Report shared: 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.
Injecting Freedom reported:
It took the FDA precisely 108 days from when Pfizer started producing the records for licensure (on May 7, 2021) to when the FDA licensed the Pfizer vaccine (on August 23, 2021). Taking the FDA at its word, it conducted an intense, robust, thorough, and complete review and analysis of those documents in order to assure that the Pfizer vaccine was safe and effective for licensure. While it can conduct that intense review of Pfizer’s documents in 108 days, it now asks for over 20,000 days to make these documents available to the public.
So, let’s get this straight. The federal government shields Pfizer from liability. Gives it billions of dollars. Makes Americans take its product. But won’t let you see the data supporting its product’s safety and efficacy. Who does the government work for?