Pfizer already hired 600 new employees because of the significant increase in side effects reports.
The employees have been hired after the C-19 vaccine was authorized in the US because of the large increase of side effects reports connected to the vaccine.
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The document adds that Pfizer has “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.”
From the first quarter of 2021, when the document was sent to the US FDA, Pfizer had 600 extra full-time workers to handle the increase.
“More are joining each month with an expected total of more than 1,800 additional resources by the end of June 2021,” Pfizer stated.
Finally got the unredacted version of this FoIA’d document. Three months after the release of the vaccine Pfizer had to hire 600 additional full-time employees, with a plan to hire 1800 total, just to process the flood of adverse events reported. pic.twitter.com/5emJ0s9djl
— Aaron Kheriaty, MD (@akheriaty) April 4, 2022
The document’s title was “cumulative analysis of post-authorization adverse event reports” of Pfizer’s shot obtained through February 28, 2021. The FDA approved it on April 30, 2021.
The document wasn’t publicized until the Public Health and Medical Professionals for Transparency sued the FDA, once the agency stated it needed decades to produce the documents linked to the EUA granted to Pfizer for the shot.
According to the February agreement, the FDA must produce a specific number of pages per month.
The side effects reports analysis was already disclosed to the health transparency group, but some segments were redacted, among which was the number of workers that have to handle the increase of side effects reports.
“We asked that the redactions on page 6 of this report be lifted, and the FDA agreed without providing an explanation,” Aaron Siri, the lawyer who represents the plaintiffs, stated for the Epoch Times.
Once the document was created, the FDA stated that the three redactions on that page could be lifted.
The redactions have been created under (b) (4) of the Freedom of Information Act, which allows agencies “withhold trade secrets and commercial or financial information obtained from a person which is privileged or confidential.”
From the unredacted version of the document, we can see that 126 million doses of the Pfizer shot were distributed worldwide once the company obtained the first clearance from the US regulators on December 1, 2020. The shipments happened through February 28, 2021.
No one knows how many of those doses had been applied!
Moreover, Pfizer didn’t respond to the emails, and there was asked how many workers it had onboarded to deal with the side effects.
The rest of the companies that received an emergency use authorization, like Moderna and Johnson and Johnson, didn’t respond whether they had seen an increase in side effects and hired more workers to deal with the reports.
The number of post-vaccination adverse reactions in VAERS spiked once the vaccines were cleared.
The most common problems were heart inflammation, blood clotting, and severe allergic shock.