Print Page | Close Window

FOIA forces FDA Pfizer vaxx data release.

Printed From: Avian Flu Talk
Category: Main Forums
Forum Name: General Discussion
Forum Description: (General discussion regarding the next pandemic)
URL: http://www.avianflutalk.com/forum_posts.asp?TID=44463
Printed Date: April 26 2024 at 1:04am


Topic: FOIA forces FDA Pfizer vaxx data release.
Posted By: A-I
Subject: FOIA forces FDA Pfizer vaxx data release.
Date Posted: December 06 2021 at 7:30pm

Pfizer COVID Jab Killed More Than 1200 People Within 90 Days, FDA Document Reveals

A trove of documents reporting on Pfizer's COVID vaccine has been released by the U.S. Food and Drug Administration (FDA) after a federal court ordered them to comply with a Freedom of Information Act (FOIA) request filed by a government accountability alliance called Public Health and Medical Professionals for Transparency (PHMPT).

PHMPT is composed of over 30 professors and scientists, who requested the federal government to share the documents that helped them decide to grant approval to Pfizer's COVID vaccine. While the FDA initially refused, claiming it would take them 55 years to review all 329,000 pages of documents, a first batch has been released and it reportedly shows some dire statistics.

According to the  https://www.thegatewaypundit.com/2021/12/court-orders-fda-comply-foia-release-information-pfizer-eua-first-batch-documents-shows-1200-vaccine-deaths-within-first-90-days/" style="box-sizing: border-box; border: 0px none; list-style: outside none none; margin: 0px; outline: none 0px; padding: 0px; -webkit-font-smoothing: antialiased; color: rgb(25, 77, 135); text-decoration: underline; - The document only included adverse effects to Pfizer's COVID vaccine that researchers believed to be "serious cases," implying that there were thousands more left out of the data. The report said that any cases deemed "non-serious" would be processed within 90 days, but the document was released before 90 days of Pfizer's COVID vaccine being available to the public.

"Due to the large numbers of spontaneous adverse event reports received for the product, the MAH has prioritised the processing of serious cases, in order to meet expedited regulatory reporting timelines and ensure these reports are available for signal detection and evaluation activity," the document read. "Non-serious cases  are processed as soon as possible and no later than 90 days from receipt. Pfizer has also taken multiple actions to help alleviate the large increase of adverse event reports."

https://www.christianitydaily.com/articles/14148/20211203/pfizer-covid-jab-killed-more-than-1200-people-within-90-days-fda-document-reveals.htm - https://www.christianitydaily.com/articles/14148/20211203/pfizer-covid-jab-killed-more-than-1200-people-within-90-days-fda-document-reveals.htm

https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf - https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf

https://phmpt.org/wp-content/uploads/2021/11/091621-Complaint.pdf - https://phmpt.org/wp-content/uploads/2021/11/091621-Complaint.pdf



-------------
"Facts don't care about your feelings" I'M A UNVAXXED DEVIL so kiss my rebel ass.



Replies:
Posted By: KiwiMum
Date Posted: December 06 2021 at 7:41pm

No wonder they are stalling about releasing their research info.



-------------
Those who got it wrong, for whatever reason, may feel defensive and retrench into a position that doesn’t accord with the facts.


Posted By: A-I
Date Posted: December 06 2021 at 7:44pm

Originally posted by KiwiMum KiwiMum wrote:

No wonder they are stalling about releasing their research info.

And no wonder the MSM is not reporting on it. And that was just the first 3 months.



-------------
"Facts don't care about your feelings" I'M A UNVAXXED DEVIL so kiss my rebel ass.



Print Page | Close Window