Changes

===FDA requests 75 years to comply===

===FDA requests 75 years to comply===

The U.S. Food & Drug Administration (FDA) asked for 75 years to fully release redacted versions of all documents related to the FDA'sa approval of Pfizer’s Comirnaty COVID-19 vaccine.  This would mean the entire cache of documents would not be fully released until 2096. The FDA’s initial timeline would have meant the release of the documents would not be completed until 2076, or 55 years from now.   

The U.S. [[Food & Drug Administration]] (FDA) asked for 75 years to fully release redacted versions of all documents related to the FDA'sa approval of Pfizer’s Comirnaty COVID-19 vaccine.  This would mean the entire cache of documents would not be fully released until 2096. The FDA’s initial timeline would have meant the release of the documents would not be completed until 2076, or 55 years from now.   

In a filing submitted to a federal judge in November 2021, the Biden [[Department of Justice]] (DOJ), arguing on behalf of the FDA, initially claimed the agency could process some 329,000 pages of documents at a rate of only 500 pages per month, in order to have time to redact legally exempt material.  According to the DOJ, such material includes “confidential business and trade secret information of Pfizer or BioNTech and personal privacy information of patients who participated in clinical trials.”

In a filing submitted to a federal judge in November 2021, the Biden [[Department of Justice]] (DOJ), arguing on behalf of the FDA, initially claimed the agency could process some 329,000 pages of documents at a rate of only 500 pages per month, in order to have time to redact legally exempt material.  According to the DOJ, such material includes “confidential business and trade secret information of Pfizer or BioNTech and personal privacy information of patients who participated in clinical trials.”

===FDA knew of risks of death===

===FDA knew of risks of death===

The first tranche of documents from a Freedom of Information Act (FOIA) request to the [[Food and Drug Administration]] (FDA) reveal that, as of February 2021, when Pfizer’s shot was being rolled out worldwide on an emergency basis,<ref>https://uncoverdc.com/2021/12/13/first-cache-of-secret-pfizer-docs-show-fda-knew-of-death-risk/</ref> the drugmaker had compiled more than 42,000 case reports detailing nearly 160,000 adverse reactions to the jab.<ref>https://www.investmentwatchblog.com/pfizer-document-shows-160000-adverse-reactions-to-vax-in-initial-months-of-rollout/</ref>

The first tranche of documents from a Freedom of Information Act (FOIA) request to the Food and Drug Administration (FDA) reveal that, as of February 2021, when Pfizer’s shot was being rolled out worldwide on an emergency basis,<ref>https://uncoverdc.com/2021/12/13/first-cache-of-secret-pfizer-docs-show-fda-knew-of-death-risk/</ref> the drugmaker had compiled more than 42,000 case reports detailing nearly 160,000 adverse reactions to the jab.<ref>https://www.investmentwatchblog.com/pfizer-document-shows-160000-adverse-reactions-to-vax-in-initial-months-of-rollout/</ref>

These reactions ranged from mild to severe, and 1,223 were fatal. The majority of these case reports involved people aged between 31 and 50 in the United States.

These reactions ranged from mild to severe, and 1,223 were fatal. The majority of these case reports involved people aged between 31 and 50 in the United States.