1.) On August 27, 2021, a FOIA request was sent to the FDA requesting the release of "All data and information for the Pfizer Vaccine."
Below is an image of the first page of the FOIA request, and you can download the full document here:
2.) On September 9, 2021, the FDA denied the FOIA request. On September 16, 2021, a lawsuit was filed against the FDA for the release of the documents.
Below are images of the first two pages of the lawsuit, and you can download the full document here:
3.) The Pfizer document was finally released and shows 158,893 adverse events in just the first 3 months of the vaccines release.
Below is an image of page 6 of the document, and you can download the full document here:
Here are some important quotes
from the Pfizer document on Adverse Events:
"Due to the large numbers of spontaneous adverse event reports received for the product, the MAH (Marketing Authorization Holder) has prioritised the processing of serious cases."
It sounds like they had more adverse events than expected. Let's read on.
"Pfizer has also taken multiple actions to help alleviate the large increase of adverse event reports. This includes significant technology enhancements, and process and workflow solutions, as well as increasing the number of data entry and case processing colleagues."
So, they had to hire more people and build more technology platforms because there were so many more adverse reactions than expected??? That's what it sounds like.
"Reports are submitted voluntarily, and the magnitude of underreporting is unknown."
So, there may have been an unknown number of additional adverse events that may have injured or killed an unknown number of people???
