A United States District Judge in Texas; Mark T. Pittman, on Thursday, January 9th, 2022, ruled that the Federal Drug Administration (FDA) must significantly accelerate the release of documents submitted to it by Pfizer to license its supposed Safe and Effective Covid-19 Vaccine.
In response to a Freedom of Information Act request for access to the documents, the FDA had asked permission to produce the documents at a rate of 500 pages per month, at which pace it would have taken over 75 years to produce all the documents.
The court; however, rejected the FDA’s request, ruling that the FDA must produce 55,000 pages per month, such that all the data could be public by the end of Summer 2022.
In the Ruling, Judge Mark T. Pittman addressed the FDA’s assertion that it lacked the manpower necessary to produce the documents at a faster rate.
“The Court recognizes the ‘unduly burdensome’ challenges that this FOIA request may present to the FDA.”
Judge Mark T. Pittman concluded that this FOIA request is of paramount public importance.”
In just 3 months; from December 2020 through February 2021, out of more than 45,000 medical trial participants, 42,086 people experienced some form of adverse effect.
1,223 participants died.
