A confidential Pfizer COVID-19 vaccine adverse event report to the FDA dated April 3, 2021 obtained by The Daily Jot possibly sheds light on why the FDA wants 75 years to release vaccine data, and why Pfizer filed in federal court to work with FDA to ensure “proper redactions are made.” The report, “5.3.6 CUMULATIVE ANALYSIS OF POST-AUTHORIZATION ADVERSE EVENT REPORTS OF PF-07302048 (BNT162B2) RECEIVED THROUGH 28-FEB-2021,” indicates as of February 28, 2021 there were 42,086 reports of 158,893 adverse events caused by the Pfizer COVID vaccine—all withheld from the public. The report’s data indicates far greater long-term risks than was ever made public.
Pfizer reported, “Pfizer’s safety database contains cases of AEs (Adverse Events) 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.” Reported side effects on pregnant women, heart conditions, blood clots, anaphylactic shock, and lack of efficacy were withheld from the public as the government propagandized that the vaccine was “safe and effective.” In fact, the Appendix of the report listed 9 pages–472 lines and 2072 words–of “Adverse Events of Special Interest.”
Some of the results: “Pregnancy outcomes for the 270 pregnancies were reported as spontaneous abortion (23), outcome pending (5), premature birth with neonatal death, spontaneous abortion with intrauterine death (2 each), spontaneous abortion with neonatal death, and normal outcome (1 each).” These represented 11.8% of the pregnancy outcomes in the database. Pfizer concluded: “There were no safety signals that emerged from the review of these cases of use in pregnancy and while breast feeding.” All along, CDC maintains on its website “COVID-19 vaccination is recommended for people who are pregnant, breastfeeding, trying to get pregnant now, or might become pregnant in the future.” Other results included: Anaphylaxis in 54% of the relevant cases retrieved, four causing death, and Pfizer concluded that the data “did not reveal any significant new safety information.”
Lack of efficacy was found in 3.9% of the cases. In the footnotes, Pfizer states that an additional 623 lack of efficacy cases were removed from the database analysis, the majority of them because they “developed SARS-CO-V-2 during the early days from the first dose.” In other words, the vaccine didn’t work, so they fudged the data. Some 3.3% of the total database developed cardiovascular adverse reactions, and “136 (9.69%) were fatal.” Again, Pfizer concluded: “This cumulative case review does not raise new safety issues.” No wonder FDA wants 75 years to release this data. The side effects of these vaccines can be devastating. Safe and effective, as the CDC adamantly claims, is not true. As Christ said in Matthew 24:4, “Take heed that no man deceive you.” These deceptions can be life-threatening.
Read the report here:
https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf
