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/ 







War Room: Dr. Naomi Wolf Reports Vaccine Dangers for Unborn Babies Are Becoming Clearer

by Linnea Wahl, Team 5 (War Room group led by Dr. Naomi Wolf)

In this video, volunteer Linnea Wahl from Team 5 discusses dangers faced by vaccinated, pregnant women and their babies. Are pregnant women who get the Pfizer mRNA vaccine putting their unborn babies at increased of dying? DailyClout’s Team 5 looks at the Pfizer data and answers this question.




WHO Initiating The Greatest Power Grab in History

By Jan Markell

If you feel like you wake up to a stunning shock daily, you’re not alone. But this story was flying under the radar until a few people blew the whistle, starting with former Congresswoman Michele Bachmann and journalist Leo Hohmann. 
 
In a few days, the World Health Organization (WHO), with assistance from the Biden Administration, is set to vote on a provision that could give this organization control of the health directives of 193 countries around the world. If passed, it could allow communist China, which controls the WHO, to dictate our national health decisions.
 
Simply stated, in the name of public health, the Biden administration plans to literally hand over America's national sovereignty to the World Health Organization when the next health emergency hits—and such an emergency is waiting in the wings.

According to Politico’s health beat reporters, the U.S. has been in “backdoor negotiations” with the WHO since January about a “treaty” that gives the WHO “greater powers to act” during a medical crisis.
 
Is this just another scheme by the global elite who are now very drunk on power and control? Even in one’s wildest imagination they cannot comprehend the danger of a foreign entity seizing control of one of our most important and even precious possessions—a nation’s healthcare.
 
Leo Hohmann writes, “By amending an existing health treaty called the International Health Regulations of 2005 (IHR), they are able to bypass U.S. Senate approval, which means no public debate and no media coverage of this sovereignty-killing power grab. It will all be done under the cloak of darkness in Switzerland, when the WHO World Health Assembly meets May 22-28.”

Hohmann says, “If the United Nations World Health Organization gets the desired new powers that the Biden administration has proposed to give it, look out. These 13 proposed amendments would create a beast with teeth at the United Nations.

“Let’s be clear on what’s happening. They are building the infrastructure for global governance and strengthening the infrastructure that’s already in place.”

The writer states, “If Biden and his Health and Human Services chief, Xavier Baccera, get their way, the nations of the world will not have their sovereignty snatched away. No, they will hand it over.

Hohmann concludes, “The vote takes place May 22-28 in Geneva, Switzerland. All that’s required is a simple majority vote and poof, there goes the sovereignty of 194 nations of the world over matters of ‘public health emergencies,’ which could include a wide range of issues, not just viruses.”

Have you seen images of the Chinese locked in their apartments pleading for help? That can be duplicated around the world under the direction of the World Health Organization. The American lock down of a year ago is minor compared to what these globalists and the WHO plan for the world.

Simply stated by Bachmann, “The Biden administration is bringing amendments that would propose that all nations of the earth cede their sovereignty over national healthcare decisions to the World Health Organization.”

Keep in mind that another 193 nations would also would lose their sovereignty to the World Health Organization as well. This organization is a subsidiary of the Chinese Communist Party who would then have authority over the U.S. and these many other nations.

The Gatestone Institute calls this a death trap for America. Gatestone Institute states that, “Unfortunately, this ‘next pandemic’ is neither far off nor a hypothetical ‘conspiracy theory.’ According to multiple credible reports from the U.S. Department of State, to the executive director of the Australian Strategic Policy Institute, Peter Jennings, China has been preparing for bio-warfare using pathogens for more than six years.

They conclude, “Unfortunately, the WHO already has proven itself to be a willing organ of China's Communist leaders. Providing it with international, legal binding authority over global pandemic response must never be allowed to happen.”

The Biden administration's amendment will make the U.S. legally obligated by international treaty to follow whatever the WHO decides.

The sweeping new powers will be invested in the Director-General of WHO to act on his own. The Director-General is Tedros Adhanom Ghebreyesus, commonly known as Tedros. Tedros, the first non-physician director-general of WHO, is an extremely controversial Marxist activist and politician from Ethiopia installed by the Chinese Communist Party.

During the pandemic itself, the American public witnessed their federal, state, and local governments forcibly shut down tens of millions of businesses, churches, and schools in fear of a virus that, in reality, proved to have a survival rate of 99%. That authority would presumably fall to the WHO under the new treaty.

The World Health Organization is working on a Vaccination Credential Initiative to implement "vaccine certificates" that can be authenticated across international borders.

The globalists are having a field day! Gaining inches some days and miles the next, they are marching toward their one-world system more each day. The four horsemen of the apocalypse are out of the barn but cannot show up until the Church is Raptured.

Write your reps in Washington although even those on the right have been silent about this pending outrage by the WHO.

Prayer may be the best weapon we have at this point. It says in Psalm 2 that God sits in the Heavens and laughs at the schemes of wicked men.






NIH Director Confirms Agency Hid COVID Genes on Orders from the Chinese

By Eric Lendrum


On Wednesday, Lawrence Tabak, the acting director of the National Institutes of Health (NIH), confirmed during congressional testimony that officials at the NIH deliberately withheld crucial information about early genomic sequences of the COVID-19 virus on the orders of Chinese scientists.

As reported by the New York Post, Tabak told the House Appropriations subcommittee that the agency “eliminated from public view” all the data from the location of the virus’s origin, Wuhan, while adding that researchers can still access the information through a “tape drive.”

When asked by Rep. Jaime Herrera Beutler (R-Wash.) why the NIH would take orders from the Chinese, Tabek responded by admitting that “there’s no question that the communication that we had about the sequence archive — Sequence Read Archive — could have been improved. I freely admit that,”

“If I may, the archive never deleted the sequence, it just did not make it available for interrogation,” Tabek added.”

“So wait, you have the information still?” Beutler then asked.

“We have the information,” Tabek responded. “Anybody who submits to the Sequence Read Archive is allowed to ask for it to be removed. And that investigator did do that. But we never erase it.”

The congresswoman followed up with another question confirming that the information was never fully erased, but instead hidden from public view, which Tabek confirmed.

Vanity Fair initially reported that the information in question could have ultimately determined whether or not the virus was formed naturally, or if it originated from the Wuhan Institute of Virology (WIV); this debate remains highly contentious in the United States and around the world, although other evidence seems to point to the WIV as the more likely origin of the virus that has since spread across the globe.