Exactly. What right do the people have to be informed as to the Federal Government's activity.
Uppity serfs.
"Let them eat Vax".
FDA Releases Pfizer’s Vaccine Adverse Reaction Data Revealing Women, People Aged 31 to 50 Suffered Most Side Effects
An FDA release of Pfizer’s internal pharmacovigilance reports on vaccine adverse reactions for its novel, gene therapy Coronavirus Disease 2019 (COVID-19) vaccine reveal women who suffered significant side effects outnumbered men by a ratio of more than 3:1, and that the bulk of reactions afflicted people of both genders aged 31 to 50.
The data was released by the Public Health and Medical Professionals for Transparency (PHMPT), a non-profit composed of 80 individuals that are mostly medical professionals.
55 long years
The PHMPT says on its website that it filed a FOIA request with the FDA on Aug. 23 after Pfizer was granted approval to distribute its injection to youth aged 16+ for “all of the data within Pfizer’s COVID-19 vaccine biological product file.”
During the filings, the organization specifically requested expedited processing, which it notes in its application letter that United States Code allows for.
The FDA denied the PHMPT expedited processing, saying that the application did “not demonstrate[] a compelling need that involves an imminent threat to the life or physical safety of an individual” or “that there exists an urgency to inform the public concerning actual or alleged Federal Government activity,” according to filings.
Aaron Kheriaty, MD
@akheriaty
I submitted this FOIA request to the FDA: they now claim it will take them 55 years to release the data on which Pfizer’s vaccine approval was based, though it only took them 108 days to review this data for the approval process. New heights of absurdity.
As a result, the PHMPT lodged a lawsuit on Sept. 16 in the U.S. District Court of Texas, seeking to compel the Agency to fulfill the request.
In mid November, the Department of Justice, which represents the FDA, told the courts it would need 55 years to review and redact information from the 329,000 pages of documents on hand at a rate of 500 pages per month.
Lawyers for the DOJ told the courts the government entity that processes FOIA requests only has ten staff members and is sitting on 400 applications, according to Reuters,
The article said Judge Mark Pittman, who presides over the case, set a conference date for Dec. 14 “to consider the timeline for processing the documents.”
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FDA Files: 26,000 ‘Nervous System Disorders’ From Pfizer Vaccine In First 2.5 Months
Added by Mark Caviezel on November 26, 2021.
Saved under Health, National
Tags: Art Moore, FDA, first responders, Nervous Disorders, Pfizer, Vaccine mandate, VAERS, WND News Center
Files released by the Food and Drug Administration in a Freedom of Information lawsuit recorded 158,893 adverse events from the Pfizer vaccine in the first two and a half months of distribution, including 25,957 incidents of “nervous system disorders.”
The documentation was obtained in a Freedom of Information lawsuit filed a group called Public Health and Medical Professionals for Transparency, comprised of more than 30 professors and scientists from universities including Yale, Harvard, UCLA and Brown.
As WND reported, in court papers filed last week, the FDA proposed that it be given 55 years to release all 329,000 pages of documents related to the Pfizer COVID-19 vaccine requested by the group.
The plaintiffs want the records so they can be assured, amid significant public skepticism, that the Pfizer vaccine is indeed “safe and effective.”
Aaron Siri, an attorney for the plaintiffs, argued in court papers filed last week that 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.”
Siri, who wants the FDA to release all the material no later than March 3, 2022, wrote in a piece published on Substack that the adverse effects were reported in a document titled “Cumulative Analysis of Post-Authorization Adverse Event Reports of [the Vaccine] Received Through 28-Feb-2021.”
On page 6 of the document, Pfizer explains: “Due to the large numbers of spontaneous adverse event reports received for the product, [Pfizer] has prioritised the processing of serious cases.”
The document says Pfizer “has also taken a [sic] multiple actions to help alleviate the large increase of adverse event reports,” including “increasing the number of data entry and case processing colleagues” and “has onboarded approximately [REDACTED] additional fulltime employees (FTEs).”
Exactly. What right do the people have to be informed as to the Federal Government's activity.
Uppity serfs.
"Let them eat Vax".
Thank you Jane!
BKMK. Thanks for additional data.