Pfizer recorded so many adverse events that it had to hire 2,400 more employees to handle paperwork and data processing

04/07/2022 / By Arsenio Toledo

Recently released Pfizer documents revealed that the Big Pharma company had to hire thousands of additional full-time employees to process the deluge of adverse reactions caused by its Wuhan coronavirus (COVID-19) vaccine.

The Food and Drug Administration (FDA) was recently ordered by a judge in Texas to accelerate the release of confidential documents passed on to the agency by Pfizer regarding its dangerous COVID-19 vaccine. (Related: Leaked top-secret Pfizer document shows COVID-19 vaccine is FAR MORE DANGEROUS than the world knows.)

The latest batch of Pfizer documents, released on April 1, is made up of 11,043 pages worth of data, including an unredacted version of the company’s post-marketing experience report.

In one of the released documents, titled “Cumulative Analysis of Post-Authorization Adverse Event Reports,” written on April 30, 2021, Pfizer admitted that it was receiving so many adverse event reports regarding its ineffective vaccine that it had to hire an additional 2,400 employees to help the company with the additional data processing and paperwork requirements.

The document stated: “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. To date, Pfizer has onboarded approximately 600 additional full-time employees. More are joining each month with an expected total of more than 1,800 additional resources by the end of June 2021.”

Pfizer’s mRNA COVID-19 vaccine is dangerous

The data uncovered from the Pfizer and FDA documents prove two things that many health freedom advocates have already known about since the beginning. First, Pfizer’s mRNA COVID-19 vaccine is dangerous.

Second, and perhaps more important, the unprecedented number of reported adverse events proved that Pfizer and the FDA knew from the beginning that the vaccine is deadly, and yet they did not disclose any of this critical information to the public.

The document also shows that, by Pfizer’s estimates, between Dec. 1, 2020 and Feb. 28, 2021, the company shipped over 126 million doses of its COVID-19 vaccine worldwide.

“The rollout of the Pfizer vaccine has led to an unprecedented number of adverse events reported – 158,000 adverse events in the first two-plus months of the rollout means that the rate of reported adverse events was approximately one for every 1,000, with many of the adverse events graded as serious,” remarked Brian Hooker, chief scientific officer of Children’s Health Defense. “It is no wonder that an army of individuals was needed to process all of the information.”

“People have been injured and died as a result of the most extensive cover-up campaign in U.S. history,” noted Mat Staver, founder and chairman of Liberty Counsel, a legal organization that specializes in defending religious freedoms. “These COVID shots are neither safe nor effective and the truth has been censored and the public has been fed lies by the U.S. government, the drug companies and the media. This is a crime against humanity.”

More Pfizer vaccine documents still to be released

As part of the FDA’s court case, all of Pfizer’s vaccine documents that it presented to the government agency should be available to the public within the next seven months.

This recent tranche of Pfizer documents also revealed some more startling information.

In some of the documents, Pfizer commissioned peer-reviewed scientific articles to claim that the Big Pharma company should continue developing and evaluating its mRNA vaccine despite the appearance of serious adverse effects among many of the trial participants.

Many of the other documents include mundane information, such as documents outlining Pfizer’s randomization scheme for identifying vaccine trial participants; documents to aid in identifying who received actual doses or the placebo; and documents listing the demographic characteristics of trial participants.

Other documents released include a questionnaire trial participants were required to complete as well as clinical study approval forms, consent forms and audit certificates for vaccine trial locations.

Learn more about Pfizer’s experimental and deadly COVID-19 vaccine at Vaccines.news.

Watch this clip from “War Room: Pandemic” as author and journalist Dr. Naomi Wolf talks about Pfizer’s knowledge regarding the massive amount of adverse events caused by its vaccine.

This video is from The Willow channel on Brighteon.com.