THE DATA IS UNCOVERED AND THE FDA IS IN TROUBLE

As part of the Food and Drug Administration’s (FDA) Emergency Use Authorization for their Covid 19 Jab, Pfizer is responsible for the management of all post-authorization safety data and is required to provide that data to the FDA in a “Post Authorization Adverse Effects Report” including all adverse effects data.
 
According to the report, “Pfizer’s safety database contains cases of Adverse Effects (AEs) reported spontaneously to Pfizer, cases reported by the health authorities, cases published in the medical literature, cases from Pfizer-sponsored marketing programs, non-interventional studies, and cases of serious AEs reported from clinical studies regardless of causality assessment.”

This report has been hidden from the public by the FDA since March of 2021. Suddenly, last month, on November 15, 2021, the FDA asked a federal judge to give it until the year 2076 to fully release the documents in its possession tied to the approval of the Pfizer-BioNTech COVID-19 vaccine including data regarding the adverse effects of the vaccine... What?

We know this because the FDA’s request for 55 years was made in a filing as part of a Freedom of Information Act (FOIA) lawsuit by a medical transparency group. The government (FDA) told the court it has 329,000 pages of documents responsive to the FOIA request and proposed releasing 500 pages per month to allow for redactions of exempt material. At that rate, the FDA would fully release the records in question in just under 55 years. Seriously?
 
“It took the FDA precisely 108 days from when Pfizer started producing the records for licensure to when the FDA licensed the Pfizer vaccine. Taking the FDA at its word, 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. While it can conduct that intense review of Pfizer’s documents in 108 days, it now asks for over 20,000 days to make these documents available to the public.” What gives?
 
Well, my friends, the first 500 pages are in, and these people are going to jail!
 
The first report https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf  included data from December 2020 – Feb 2021 and was issued to the FDA shortly after the data was compiled, so in early March 2021. Since then, with all of the showcasing performed by the FDA, they have remained quiet until forced to release the data in the FOIA lawsuit. Shameful!
 
In the Report on page 6, it states “Among adverse event reports received into the Pfizer safety database during the cumulative period, only those having a complete workflow cycle in the safety database (Meaning they progressed to Distribution or Closed workflow status) are included in the monthly SMSR. This approach prevents the inclusion of cases that are not fully processed hence not accurately reflecting final information."

This means as bad as it is, not all AE cases are included.

"Due to the large numbers of spontaneous adverse event reports received for the product, the MAH has prioritized 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.”

This means serious cases were prioritized, so there are more than were reported. 
 
"According to the report, “cumulatively, through 28 February 2021, there was a total of 42,086 case reports (25,379 medically confirmed and 16,707 non-medically confirmed) containing 158,893 events."

This means about 4 adverse events per case...
 
"Most cases (34,762) were received from United States (13,739), United Kingdom (13,404) Italy (2,578), Germany (1913), France (1506), Portugal (866) and Spain (756); the remaining 7,324 were distributed among 56 other countries.”

This means about half of all cases reported were from the US.
 
 Withheld by the FDA - 1,227 deaths in just the first 3 months!

On page 7, the report presents the diversity of complications...a chart breaks down the greatest number of events by class:

• General disorders and administration site conditions (51,335 AEs),
• Nervous system disorders (25,957),
• Musculoskeletal and connective tissue disorders (17,283),
• Gastrointestinal disorders (14,096),
• Skin and subcutaneous tissue disorders (8,476),
• Respiratory, thoracic and mediastinal disorders (8,848),
• Infections and infestations (4,610),
• Injury, poisoning and procedural complications (5,590), and;
• Investigations (3,693).

 
I’ll let you read the rest…1,227 deaths reported in just the first 3 months! 1 out of every 37 events reported resulted in DEATH! This data is in only the first 500 pages of 369,000 the FDA said was covered by the FOIA lawsuit. Fauci and the FDA knew of these effects and did nothing but push the jab on everyone. The FDA had Pfizer's data, the FDA knew the jabs were killing people, and Fauci withheld this data. PROSECUTE!

These are not accusations, this is real data required by law in any FDA Emergency Use Authorization. Please read the data yourself. No wonder the FDA wanted to spend 55 years releasing it.

Time for accountability!​