FDA and Pfizer Knew COVID Shot Caused Immunosuppression

At A Glance

• April 1, 2022, another batch of 11,000 Pfizer documents were released by the U.S. Food and Drug Administration. Pfizer trial data reveal natural immunity was as effective as the jab, and that shot side effects were more severe in those under 55. Since the risk of severe COVID is dramatically lower in younger people, an elevated risk of side effects unacceptable, and the shot should have been restricted to those at high risk of severe COVID 

• The adverse event rate per dose for Pfizer’s mRNA jab, based on their own studies, is nearly 1 in 800, and the myocarditis rate is 10 in 100,000 — far greater than the 2 in 100,000 rate previously reported 

• Pfizer’s consent form specifies that the effect on sperm, fetuses and nursing children are unknown. Yet health authorities and media have espoused as “fact” that the shot does not affect reproductive health or fertility and is perfectly safe for pregnant and nursing mothers 

• Pfizer’s documents show they’ve not ruled out the risk of antibody-dependent enhancement. Vaccine-associated enhanced disease (VAED) is listed as an “Important Potential Risk.” As of February 28, 2021, Pfizer had 138 cases of suspected VAED, 75 of which were severe, resulting in hospitalization, disability, life-threatening consequences or death; a total of 38 cases were lethal and 65 remained unresolved 

• Pfizer and FDA also knew that people of all ages experienced transient suppression of immune function for one week after the first dose 

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