In total, Pfizer discloses the existence of 42,086 adverse event case reports containing 158,893 total events, including 1,227 deaths. 25,957 of the events were classified as “Nervous system disorders.” So for those who think that somehow VAERS is not accurate or is overreporting deaths, these are numbers straight from the horse’s mouth just through February. Remember, it is extremely hard to trace many serious events back to the vaccine, including death, especially if there is a few weeks’ lag time, and most especially with people already in advanced age. So these are just the ones that were “submitted voluntarily, and the magnitude of underreporting is unknown.”
Full stop right there. Under any other circumstance, such a vaccine would have been removed from the market right away, certainly not fully endorsed, marketed, funded, and mandated by government. It was so bad that Pfizer reveals, “Due to the large numbers of spontaneous adverse event reports received for the product, the MAH has prioritized the processing of serious cases” and also had to hire more full-time employees to handle the reporting. How was it ethical for the FDA to withhold this information from the public, and how can it ever be ethical to mandate such a shot, even if one believes that, in general, a government could wield such authority? This is especially true now that we know its efficacy is minimal at best and downright enhances the virus at worst.
On November 15, The Food and Drug Administration (FDA) asked a federal judge to give it until the year 2076 to fully release all of the data and the documents the agency used as the basis for the approval and license of the Pfizer-BioNTech COVID-19 vaccine. Now we know why.
The revelation came to light in a filing as part of a Freedom of Information Act (FOIA) lawsuit by a medical transparency group. The government told the court it has 329,000 pages of documents responsive to the FOIA request and proposed releasing 500 pages per month to allow for redactions of exempt material.
During the court hearing, The Department of Justice (DOJ) lawyers representing the FDA asked a federal judge to allow them an unthinkable 55 years to process the request, saying they would only be able to release just 500 pages a month. The court denied FDA’s request. Instead, the court ordered the FDA to comply with FOIA’s request and release the information on the Pfizer vaccine.
Now, the first batch of documents is now available for the public to see. According to an official Pfizer confidential document that is titled, “Cumulative Analysis of Post-Authorization Adverse Event Records Reports,” there were over 1,200 vaccine deaths within the first 90 days of the vaccine’s roll out under the FDA’s EUA – from December 1st. 2020 – February 28th, 2021.
In one instance, the report stated that four people died on the same day they were vaccinated.
Click link below for the full article as well as links to download the documents