It took a subpoena to do it, but we are finally getting some answers to just how safe the COVID-19 vaccines are and the answers are terrifying. On just the Pfizer vaccine within the first few months, it was available, there were 158,893 adverse reactions and 25,957 people suffered nervous system disorders. Attorney Aaron Siri, the Managing Partner of Siri & Glimstad, published the first documents that were released.
Aaron Siri has a history of representing people for vaccine injury for a very long time now and he has just released the first information that has been given to him via a subpoena. He told a panel discussion led by Sen Ron Johnson that during the COVID crisis, his law firms’ phones have been ringing off the hook with complaints related to the vaccine.
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“If we actually sued all of the pharmaceutical companies for all of the complaints it would actually impossible for all of the attorneys around the country, around 100, to handle all of those matters.”
Two months and one day after it was sued, and close to 3 months since it licensed Pfizer’s Covid-19 vaccine, the FDA released the first round of documents it reviewed before licensing this product. The production consisted of 91 pdf pages, one xpt file, and one txt file. You can download them here.
While it is for the scientists to properly analyze, let me share one observation. One of the documents produced is a Cumulative Analysis of Post-Authorization Adverse Event Reports of [the Vaccine] Received Through 28-Feb-2021, which is a mere 2 ½ months after the vaccine received emergency use authorization (EUA). This document reflects adverse events following vaccination that have completed Pfizer’s “workflow cycle,” both in and outside the U.S., up to February 28, 2021.
Pfizer explains, on page 6, that “Due to the large numbers of spontaneous adverse event reports received for the product, [Pfizer] has prioritised the processing of serious cases…” and that Pfizer “has also taken a [sic] multiple actions to help alleviate the large increase of adverse event reports” including “increasing the number of data entry and case processing colleagues” and “has onboarded approximately [REDACTED] additional fulltime employees (FTEs).” Query why it is proprietary to share how many people Pfizer had to hire to track all of the adverse events being reported shortly after launching its product.
As for the volume of reports, in the 2 ½ months following EUA, Pfizer received a total of 42,086 reports containing 158,893 “events.” Most of these reports were from the U.S. and disproportionately involved women (29,914 vs. 9,182 provided by men) and those between 31 and 50 years old (13,886 vs 21,325 for all other age groups combined, with another 6,876 whose ages were unknown). Also, 25,957 of the events were classified as “Nervous system disorders”