Secret Documents: How Pfizer Covered Up a Flood of Adverse Events

by Stevan Looney


I am a civil trial and appellate attorney in New Mexico, with experience litigating complex matters. My prior essay for DailyClout.io regarding the Pfizer WarRoom Document Review — for which I volunteer as one of 250 attorneys — argued that the documents clearly show evidence of fraud on the part of Pfizer. The latest tranche of documents, released on April 1, 2022, show an equally dramatic revelation: Pfizer knew by February of 2021, that there were had been ‘a large number of adverse events’ in the three months prior

Pfizer also realized that these adverse events were so abundant — and they expected so many more in the months to come — that they advised the FDA that they would hire 2400 additional staffers to deal with the paperwork and data processing they expected due to the anticipated volume of adverse events!  

I reviewed the April 1, 2022, tranche of Pfizer documents the FDA produced pursuant to a federal court order. A document produced on November 17, 2021, was also produced as “reissued” on April 1, 2022. At first glance they appear identical, but they are not. Importantly, information redacted (deleted) from the document produced in the March 2022 production, was included in the April 1, 2022, production. This information is quite telling and some conclusions can be drawn.

The document produced on November 17, 2021, is titled “5.3.6 postmarketing experience.pdf” (November 17, 2021 (984 KB)). That same document in the April 1, 2022, production is titled “reissue_5.3.6 postmarketing experience.pdf”. (April 1, 2022 (958 KB)). The word “reissue” is absent in the November 2021 version. That made me curious, so I did a comparison of the two documents. Here is what one will find on page 6. (The “Bates” number in both documents in the bottom, right-hand corner is “FDA-CBER-2021-5683-0000059.”)

The lengthy paragraph on page 6 of the November 2021 document concerns adverse events reports received by Pfizer as of February 28, 2021. The third sentence of that paragraph in both documents reads: “Due to the large number of spontaneous adverse events reports received for the product [i.e., BNT162b2], the MAH [Marketing Authorization Holder] has prioritized the processing of serious cases, in order to meet expedited regulatory reporting timelines and ensure these reports are available for signal detection and evaluation activity.”

This paragraph ends: “Pfizer has also taken a [sic] multiple actions to help alleviate the large increase of adverse event reports.” Think about that sentence.

“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 (FTEs). More are joining each month with an expected total of more than 1,800 additional resources by the end of June 2021 [emphasis added].”

Also on page 6, under the heading “3. RESULTS”, at “3.1.1 General Overview”, Pfizer discloses in the document produced on April 1, 2022, what it redacted from the same document produced in November of 2021. What Pfizer had produced in April 2022 to take the place of the redacted document in November 2021 document was the fact that for the three-month period beginning December 1, 2020, to February 28, 2021, Pfizer shipped “approximately 126,212,580 [emphasis added] doses of [the FDA emergency use authorized] BNT162b2″ worldwide.

The 126,212,580 figure is redacted in the document produced in November 2021 but is included in the “reissue” document of April 1, 2022.

Likewise, the new, full-time 600 and 1,800 employees, amounting to a total of 2,400 full-time employees, hired to deal with all the anticipated adverse events, are included in the document produced on April 1, 2022, but had been redacted from the same document the FDA had produced in November of 2021. Why the foregoing data were redacted, but then disclosed, we do not know, yet. We do know that the redacted information is damning. What did we learn by comparing the two documents?

First, between December 1, 2020 and February 28, 2021, a period of three months, “a large number of spontaneous adverse events reports” were made to Pfizer regarding the administration to humans of the BNT162b2 “vaccine” for which the FDA had provided emergency use authorization (EUA).

Second, by February 28, 2021, (the date of the document) Pfizer knew that by June of 2021 it would hire at least an additional 2,400 full-time employees to process the adverse events reports Pfizer was receiving. (Appendix 1 to these documents is a list of 1,290 adverse events of special interest (AESI) received in connection with the BNT162b2 “product.” Based upon my research to date, I have found no evidence that these AESI were disclosed publicly prior to November of 2021.)

Lastly, and incredibly, despite having this information, on August 23, 2021, the FDA granted continued EUA status for the BNT162b2 “vaccine” and also approved Bio-N-Tech/Pfizer’s product known as COMIRNATY. Notably, according to the FDA, both the EUA BNT162b2 and the “approved” COMIRNATY are identical and interchangeable products. Thus, it is reasonable to conclude that COMIRNATY also causes “a large number of spontaneous adverse events,” including the adverse events and AESI listed in Appendix 1 to these documents.

In sum, Pfizer did not only apparently commit fraud, but they also compounded the fraud by hiring 2,400 full-time employees to deal with the flood of adverse events that they expected – and yet they told no one about this publicly.

 I will continue to issue analyses of these historic documents.

Mr. Looney is a civil trial and appellate attorney with 42 years of experience, concentrating on complex matters.  Mr. Looney is licensed in New Mexico and practices in all its courts, as well as the United States District Court for the District of New Mexico, the Tenth Circuit Court of Appeals, the US Tax Court and the US Supreme Court.  Mr. Looney served in the U.S. Army as an infantryman from 1970-1972, assigned to the 82nd Arbrn. Div.

Article Source: https://dailyclout.io/how-pfizer-covered-up-anticipated-adverse-events/ 







Whistleblower: Pfizer FORGED signatures of trial participants, falsified and fabricated trial data

(Natural News) A former Pfizer contractor-turned-whistleblower said the Big Pharma company forged informed consent signatures and falsified and fabricated clinical trial data for its Wuhan coronavirus (COVID-19) mRNA vaccine. Brook Jackson, who has nearly 20 years of experience in clinical research for the pharmaceutical and medical … [Read More...]


Georgia hospital weaponizes Biden’s vax mandate, holds couple against their will for days

by Leo Hohmann


A petition drive may have helped save the lives of two Georgia residents who were trapped in a hospital that refused to respect their daughter’s power of attorney and release them to another medical facility that would administer critical life-saving treatments.

Joseph and Beverly Rickels were both admitted to Piedmont Hospital in Cartersville, Georgia, on Sunday, Sept. 12, diagnosed with Covid-related pneumonia. The condition of both husband and wife has now deteriorated to the point where both are receiving oxygen. Joseph is in critical condition.

LifeSite News, a conservative media organization, asked people Thursday to sign a petition requesting the governor to step in and allow the daughter to get her parents out of Piedmont Hospital and into another facility that will give the treatments they need.

Shockingly, the attending physician said that she would not release the patients to their daughter’s care unless she (the daughter) proves she is vaccinated.

See our previous article explaining how hospitals nationwide are complying with top-down CDC guidelines focused on a vaccine-exclusive approach that is actually killing people.

Word came late Friday afternoon, Sept. 17, that the petition campaign was yielding results. Officials at Piedmont Hospital had finally conceded to let the couple see any doctor of their choice who could come to the hospital and give them the treatment they requested, but that decision came days late and only after extensive public pressure had been applied on the hospital, Steve Jalsevec, president and co-founder of LifeSite News, told LeoHohmann.com.

“Crucial time was lost in dealing with their obstinance and denying the use of critical medications that are known to work all around the world, and then they wouldn’t release the patients to their daughter who had power of attorney, simply because she was unvaccinated,” Jalsevec said.

The LifeSite email alert sent out Thursday asked readers to “urgently CONTACT Governor Brian Kemp to intervene in this case and demand that Piedmont Hospital respect the power of attorney of their daughter, and the desire of Joseph and Beverly Rickels to be moved to another location to receive the care of their choice.”

The couple’s daughter, Courtney Rimmer, has power of attorney, which should, by law, allow her to make decisions for her parents, both of whom indicated they agree to the move.

You can still call or email the Governor’s Office to let him know your displeasure on how this hospital is failing its patients. The number is (404) 656-1776.

The Rickels have the right to receive fully-approved, known safe alternative treatments such as Ivermectin, and this hospital did not respect their duly-appointed power of attorney, as well as medical privacy, until it was possibly too late.

If Piedmont is denying critical treatment to the Rickels, they are likely doing the same to other Covid patients. This must stop.

It might also be a good idea to contact Georgia State Attorney General Chris Carr to ask that his office investigate the medical tyranny that is overtaking Georgia’s hospitals. The Attorney General’s number is: (404) 458-3600.

If this can happen to the Rickels, it can happen to anyone.

Piedmont Healthcare is a private nonprofit operating 16 hospitals and hundreds of clinics throughout Georgia.

The hospital chain claims on its website factsheet to “provide safe, compassionate, convenient, and high-quality care across 16 hospitals, 50 Piedmont Urgent Care centers, 25 QuickCare locations, 610 Piedmont Clinic physician practice locations and more than 2,770 Piedmont Clinic members.”

If Piedmont is truly interested in “high-quality, compassionate care,” it would not have delayed the administering of critical treatments to the Rickels. It would not need to receive dozens of calls and/or emails to remind them how to make such basic good-faith decisions. And it certainly would not be asking for the vaccine status of a worried daughter before honoring her wishes as power of attorney for her parents.

We at LeoHohmann.com are 100 percent reader supported and committed to honest, independent journalism in defense of life and liberty. We operate on a shoestring, so if you can help us, please consider a donation of any size: Send c/o Leo Hohmann, PO Box 291, Newnan, GA 30264 or by clicking the donate button below.

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Guillain Barre warning added to Johnson & Johnson Covid19 vaccine by FDA, getting it 3 to 5 times higher after vaccination

by Citizen Wells


Guillain Barre Syndrome GBS warning added to Johnson & Johnson Covid19 vaccine by FDA, Chances of getting 3 to 5 times higher after vaccination

“two papers published May 19 in the journal of Hospital Pediatrics found pediatric hospitalizations for COVID were over counted by at least 40%, carrying potential implications for nationwide figures used to justify vaccinating children.”...The Defender

“it is universally known that children virtually never die from COVID-19 and given that children have a very strong immune system, they are more likely than adults to have an over-reaction to the shot.”…Dr. Steven Roth

“There is not yet enough evidence on the use of vaccines against COVID-19 in children to make recommendations for children to be vaccinated against COVID-19. Children and adolescents tend to have milder disease compared to adults. However, children should continue to have the recommended childhood vaccines.”…WHO


From The Defender July 12, 2021.

“FDA to Add Warning to J&J Vaccine of ‘Serious But Rare’ Autoimmune Disorder

The U.S. Food and Drug Administration will announce a new warning on Johnson & Johnson’s COVID vaccine saying the shot is linked to Guillain–Barré syndrome. In April, the agency added a warning about blood clotting disorders to the J&J shot.

The U.S. Food and Drug Administration (FDA) is will announce a new warning on Johnson & Johnson’s (J&J)
COVID vaccine saying the shot has been linked to Guillain–Barré syndrome (GBS), a “serious but rare” autoimmune disorder. The Washington Post attributed the news to “four individuals familiar with the situation.”

According to The New York Times, the chances of developing GBS after receiving the J&J shot is three to five times higher than would be expected in the general population in the U.S.

About 100 preliminary reports in the U.S. of GBS have been detected after receiving J&J’s vaccine, the Centers for Disease Control and Prevention (CDC) said in a statement to CNN today. Most cases were reported about two weeks after vaccination, mostly in men 50 and older.


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