Attorney Aaron Siri, the Managing Partner of Siri and Glimstad, released the first pages from subpoenaed FDA files.
He has extensive civil litigation experience. He has represented people for vaccination injury for some time while he told a US panel discussion led by Senator Ron Johnson that in the C-19 pandemic, their phones got an avalanche of requests.
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The attorney added, “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.”
Attorney Aaron Siri shared the primary pages of subpoenaed docs from the FDA on Pfizer’s coronavirus vaccine.
From the released documents, we can see that in the first months of 2021, there were 158.893 side effects and among them were 25.957 nervous system disorders.
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”
These are the Open VAERS numbers: