FDA lawsuit first report reveals 158893 adverse events in 2.5 months, 25957 “Nervous system disorders”, Attorney Aaron Siri, European Union database shows 87639 serious nervous system disorders
“Why are we vaccinating healthy adults when 81 percent of Covid-19 cases are mild and there is a 99 percent survival rate. Why are we testing vaccines on children who are minimally impacted by the disease?”…Citizen Wells
“I’m not afraid of blowing the whistle “because my faith lies in God and not man … You know, like what kind of person would I be if I knew all of this — this is evil at the highest level. You have the FDA [U.S. Food and Drug Administration], you have the [Centers for Disease Control and Prevention] CDC, that are both supposed to be protecting us, but they are under the government, and everything that we’ve done so far is unscientific.”..Jodi O’Malley registered nurse
” if you let your healthy teen – much less your healthy child – get this vaccine, you are insane.”…Alex Berenson
From Attorney Aaron Siri.
FDA Produces the First 91+ pages of Documents from Pfizer’s COVID-19 Vaccine File
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”
Females between the ages of 30 and 51. Nervous system disorders. That sounds familiar. As a matter of fact, that sounds similar to the concerns raised by some of the women testifying or described in the videos below.”
Read more:
https://aaronsiri.substack.com/p/fda-produces-the-first-91-pages-of
“The official European Union database of suspected drug reaction website is now reporting 30,551 fatalities and 1,163,356 from COVID vaccines Pfizer, Moderna, and Johnson & Johnson, and AztraZeneca through November 13, 2021 based on the data submitted to its system.”
It also revealed 87,639 serious nervous system disorders
Read more here:
Citizen WElls 