Fri Dec 3, 2021 – 8:06 pm ESTFri Dec 3, 2021 – 8:18 pm EST
(LifeSiteNews) — Tens of thousands of serious adverse events and more than 1,200 deaths were reported in the first three months after Pfizer’s COVID-19 jab was approved under emergency use authorization (EUA), newly released documents indicate.
The data had been reviewed by the U.S. Food and Drug Administration (FDA) before it granted full approval to the Pfizer-BioNTech COVID-19 (BNT162b2) shots over the summer but had not been released to the public until last month.
The FDA released the documents on November 19, months after the governmental agency was hit with a Freedom of Information Act (FOIA) request filed by attorney Aaron Siri on behalf of a group of some 30 scientists, academics, and researchers who demanded transparency about the information that had been used to assess the safety profile of the injections.
In response, the FDA moved to challenge the group’s request in court, raising eyebrows when it asked a federal judge to grant it 55 years to fully release the documents it reviewed before ultimately granting full approval for the Pfizer shots for people age 16 and up in August.
Now the FDA has made public some 91 pages of the documents it reviewed before authorizing the Pfizer
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