FDA Docs Reveal More Than 40K Serious COVID Adverse Reactions

Besides this, another shocking info from the documents reveals 1.2K recorded deaths, that have been associated with the Pfizer COVID jab, within the very 2.5 months after it was being approved and used.

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The FDA has released 91 pages of the documents on the Pfizer shot’s safety and efficacy in 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). There are another 329,000 pages that the agency is yet to make public.

“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.

The lion’s share of all AEs — 29,914 — was seen in women, and 9,182 occurred in men. The medics did not have any data on gender in 2,990 cases.

The majority of the affected recipients, 19,582 of them, either “recovered” or were “recovering” at the time of the report. 520 “recovered with sequelae” (developed a chronic condition), 11,361 have not recovered, and 1,223 people died following the inoculation with Pfizer shot. It remained “unknown” what happened to the 9,400 patients.

The biggest number of the AEs occurred in middle-aged people of 31-50-years of age (13,886), an age group that is generally at low risk of serious effects from the disease the jab is presumably designed to prevent. That group was followed by 51-64-year-olds (7,884). There were 5,214 seniors older than 75 who got adverse reactions to the shot, and 4,953 younger people between the ages of 18 and 30.

Of all the AEs following the vaccination, the general disorders and administration site conditions place first, accounting for 51,335 AEs. Then go 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).

The report also mentioned that there are “identified” and “potential” safety concerns related to the shot.

“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.”

Though there is some hope behind these news, the timing of their release is a real tragedy.

AaronSiriPDF fileThe New AmericanAARPPHMPTMayo Clinic

Ava Garcia

A small town girl, dreaming big, expecting to change the world with presenting the truthful events of the world today. Law degree with a master in criminology, and a devoted journalist for over 7 years, and counting. "The pen is mightier than the sword."

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