FDA Docs Reveal More Than 40K Serious COVID Adverse Reactions

It’s worse than you first thought

New info reveals that 1.2K deaths caused by Pfizer jabs happened two months after the FDA approved them.

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The FDA released 91 pages of the documents on the safety and efficacy of this jab. They had to do this as a response to the lawsuit filed against the agency by an international group of medical professionals, scientists, and journalists called Public Health and Medical Professionals for Transparency (PHMPT). The agency will have to release another 329,000 pages.

“Two months and one day after it was sued, and close to three months since it licensed Pfizer’s Covid-19 vaccine, the FDA released the first round of documents it reviewed before licensing this product,” Aaron Siri, the lawyer who represents the group, wrote on his blog.

“While the released documents represent only a tiny fraction of the massive amount of the medical data on the Pfizer shot, the information revealed in the documents raises serious concerns about the actual safety of the increasingly mandated drugs that are now also actively advertised to children as young as five,” Mayo Clinic has reported.

“Among the FDA documents released is a 38-page document entitled “CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021”(pdf), which outlines the general number of all “serious” adverse events (AE) as well as information on the demographics those adverse events occurred in those countries that used the Pfizer shot.”

“Geographically-wise, “Most cases (34,762) were received from United States (13,739), United Kingdom (13,404), Italy (2,578), Germany (1913), France (1,506), Portugal (866) and Spain (756); the remaining 7,324 were distributed among 56 other countries,” per the report.

About 520 recipients “recovered with sequelae” and 11,361 didn’t recover. About 1,223 people died. So, that happened to 9,400 people?

The largest number of AEs was noticed in people aged 31-50 (13,886). People aged 51-64 are next (7,884). About 5,214 seniors older than 75 had adverse reactions and 4,953 people aged 18-30 developed symptoms.

General disorders and administration site conditions are first (51,335 AEs). Then we have 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), and injury, poisoning, and procedural complications (5,590).

According to the report, there are “identified” and “potential” safety concerns.

“Important identified risks” associated with the shot is anaphylaxis, which accounted for 1,883 AEs. Mayo Clinic defines the condition as “a severe, potentially life-threatening allergic reaction.” And also: “Anaphylaxis causes the immune system to release a flood of chemicals that can cause you to go into shock — blood pressure drops suddenly and the airways narrow, blocking breathing.”

There are also “Important potential risks,” such as Vaccine-Associated Enhanced Disease (VAED), Including Vaccine-associated Enhanced Respiratory Disease (VAERD). Per the report, “VAED may present as severe or unusual clinical manifestations of COVID-19.” This means that people who took the shot may fall ill with a severe case of COVID.

“Use in Pregnancy and lactation” is marked as a “Missing information” in the report. It is unclear why it is defined as “missing” when 413 AEs in pregnant women were reported. Eighty-four of them were “serious” and 329 “non-serious.”

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Source: The True Defender

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