Documents released by the Food and Drug Administration (FDA) reveal that drugmaker Pfizer recorded nearly 160,000 adverse reactions to its Covid-19 vaccine in the initial months of its rollout.
First bolus of Pfizer vax data from our FOIA request yields alarming adverse event findings: “Cumulatively, through 28 February 2021 [less than three months], total of 42,086 case reports (25,379 medically confirmed and 16,707 non-medically confirmed) containing 158,893 events.
— Aaron Kheriaty, MD (@akheriaty) December 12, 2021
The documents were obtained by a group of doctors, professors, and journalists calling themselves Public Health and Medical Professionals for Transparency, who filed a (FOIA) request with the FDA for their release.
The first tranche of documents reveal that, as of February 2021, when Pfizer’s shot was being rolled out, the drugmaker had compiled more than 42,000 case reports detailing nearly 160,000 adverse reactions to the jab.
These reactions ranged from the mild to the severe, and 1,223 were fatal. The majority of these case reports involved people aged between 31 and 50 in the United States.
More than 25,000 nervous system disorders were reported, along with 17,000 musculoskeletal and connective tissue disorders and 14,000 gastrointestinal disorders. A range of different autoimmune conditions were reported, along with some peculiar maladies, including 270 “spontaneous abortions,” and incidences of herpes, epilepsy, heart failure and strokes, among thousands of others.
And the link to all the currently available Pfizer documents. In the latest round of nonsense, the company is now requesting 75 years (rather than the original 55 years) to release all the Pfizer data publicly. We’ll see what the federal judge thinks. https://t.co/wilLaVowSk
— Aaron Kheriaty, MD (@akheriaty) December 12, 2021
Take a look at “APPENDIX 1. LIST OF ADVERSE EVENTS OF SPECIAL INTEREST” which goes on for 9 very dense pages.
— Aaron Kheriaty, MD (@akheriaty) December 12, 2021
BREAKDOWN OF AESI’s
Definition of Adverse Events of Special Interest: An adverse event of special interest (serious or nonserious) is one of scientific and medical concern specific to the sponsor’s product or program, for which ongoing monitoring and rapid communication by the investigator to the sponsor can be appropriate. Such an event might warrant further investigation in order to characterize and understand it. Depending on the nature of the event, rapid communication by the trial sponsor to other parties (e.g., regulators) might also be warranted (Based on CIOMS VI).
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