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.
"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 difficult to imagine a greater need for transparency than immediate disclosure of the documents relied upon by the FDA to license a product that is now being mandated to over 100 million Americans under penalty of losing their careers, their income, their military service status, and far worse."
"We assume, as the FDA has stated, that 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."
"The FDA now has an equally important task of making those documents available to the Plaintiff in this case and the public at large in at least the same timeframe," the filing adds.
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