Pfizer Whistleblower Sinks Vaccine Trial Integrity

STORY AT-A-GLANCE

• According to a whistleblower who worked on Pfizer’s Phase 3 COVID jab trial, data were falsified, patients were unblinded, the company hired poorly trained people to administer the injections, and follow-up on reported side effects lagged way behind

• Brook Jackson was the regional director of Ventavia Research Group, a research organization charged with testing Pfizer’s COVID jab at several sites in Texas. Jackson repeatedly “informed her superiors of poor laboratory management, patient safety concerns, and data integrity issues,” and when her concerns were ignored, she finally filed a complaint with the U.S. Food and Drug Administration

• The FDA did not follow up on her complaint. Ventavia was not one of the nine trial locations audited, and Pfizer did not bring any of those issues up when applying for emergency use authorization for its COVID shot

• Documentation shared by Jackson shows a Ventavia executive had identified three site staff members who had falsified data

• After being notified of Jackson’s complaints, Pfizer contracted Ventavia to conduct four additional trials — one for COVID shots in children and young adults, one for the COVID jab in pregnant women, a booster shot trial, and an RSV vaccine trial

Yet again, mainstream media have completely ignored what should have been front-page news. According to a whistleblower who worked on Pfizer’s Phase 3 COVID jab trial in the fall of 2020, data were falsified, patients were unblinded, the company hired poorly trained people to administer the injections, and follow-up on reported side effects lagged way behind.

What makes the media’s silence all the more remarkable is that this revelation was published in The British Medical Journal. Paul Thacker, investigative journalist for The BMJ, writes in his November 2, 2021, report:1

As noted by Bill Bruckner for transparimed.org:2

So far, this story has been largely confined to the alternative news media. You’ll find a selection of video reports covering the whistleblower’s testimony in the sections below.

Research Organization Falsified Data in Pfizer Trial

The whistleblower in question is Brook Jackson, a former regional director of Ventavia Research Group, a research organization charged with testing Pfizer’s COVID jab at several sites in Texas.

Jackson repeatedly “informed her superiors of poor laboratory management, patient safety concerns and data integrity issues,” Thacker writes, and when her concerns were ignored, she finally called the U.S. Food and Drug Administration and filed a complaint via email.

Jackson was fired later that day after just two weeks on the job. According to her separation letter, management decided she was “not a good fit” for the company after all. She has provided The BMJ with “dozens of internal company documents, photos, audio recordings and emails” proving her concerns were valid. According to Jackson, this was the first time she’d ever been fired in her 20-year career as a clinical research coordinator. Thacker explains:3

FDA Ignored Whistleblower Concerns

In her complaint to the FDA, Jackson listed a dozen incidents of concern, including the following:

• Participants were not monitored by clinical staff after receiving the shot

• Patients who experienced adverse effects were not promptly evaluated

• Protocol deviations were not being reported

• The Pfizer injection vials were stored at improper temperatures

• Laboratory specimens were mislabeled

Not a single one of the problems Jackson raised in her complaint to the FDA were noted or addressed in Pfizer’s briefing document submitted to the FDA’s advisory committee meeting December 20, 2020, when its emergency use authorization application was reviewed.

The FDA went ahead, granting the Pfizer jab emergency use authorization the very next day, despite being in receipt of Jackson’s complaint, which ought to have put the brakes on the FDA’s authorization. At bare minimum, they should have investigated the matter before proceeding.

What’s more, the FDA’s summary of its inspections of the Pfizer trial, published in August 2021, revealed the agency only inspected nine of the 153 trial sites, and Ventavia was not one of them. The complaint also appears to have been ignored when the FDA granted full approval to Comirnaty, Pfizer/BioNTech’s COVID shot that is not yet available.

Pfizer is also in on the cover-up. Shortly after Jackson’s firing, Pfizer was notified of the problems she’d raised. Despite that, Pfizer has since then contracted Ventavia to conduct no less than four additional trials — one for COVID shots in children and young adults, one for the COVID jab in pregnant women, a booster shot trial, and an RSV vaccine trial.

So, clearly, Pfizer is not opposed to contractors falsifying data or otherwise undermining the integrity of the trials. That alone is a fiery indictment against Pfizer.

They can feign ignorance and proclaim to adhere to “the highest scientific, ethical and clinical standards”4 all they want. Those are just words which, unless backed by consistent action, are completely meaningless. Behind the scenes, they’re clearly well-aware that their trials are resting on fraudulent foundations.

Pfizer Trial Described as a ‘Crazy Mess’

Jackson wasn’t the only employee to get sacked from Ventavia after raising concerns about the integrity of the Pfizer trial. Thacker writes:5

Such statements clearly fly in the face of statements made by world leaders, health authorities and the mainstream media. Most, like federal health minister for Australia, Greg Hunt, have claimed the COVID shots have undergone “rigorous, independent testing” to ensure they’re “safe, effective and manufactured to a high standard.”6

Nothing we know so far supports such a conclusion. The testing has been far from rigorous and has not been independently verified.

Vaccine Adverse Events Reporting System (VAERS) data show they’re shockingly far from safe; real-world data show effectiveness wanes within a handful of months while leaving you more susceptible to SARS-CoV-2 variants and other infections; and manufacturing standards have also been shown lacking, as a variety of foreign contaminants have been found in the vials.7

Media Are Manipulated by Pfizer

One of the reasons why English- and German-speaking legacy media have completely ignored this whistleblower testimony is probably because Pfizer has such a dominating influence over them. Thacker told blogger Maryanne Demasi, Ph.D.,8 “Pfizer has such a huge PR machine, they have basically captured the media, they’ve hypnotized the media.”

Pfizer’s PR department is also hard at work trying to hypnotize the public. The TV ad above is perhaps one of the most offensive. In it, Pfizer brainwashes young children into thinking that getting the COVID shot will make them superheroes. Never mind the fact that getting the shot could kill or permanently injure them.

You Cannot ‘Follow the Science’ if There Are No Data

The video at the top of this article is a short extract from a November 2, 2021, meeting organized by Sen. Ron Johnson, during which associate editor of The BMJ, Peter Doshi, Ph.D., reviewed some of the many concerns experts have about the integrity of the COVID jab data.

He points out that Pfizer’s raw trial data will not be made available until May 2025. So far, Pfizer has refused to release any of its raw data to independent investigators and, without that, there’s no possible way to confirm that what Pfizer is claiming is actually true and correct.

In other words, we’re expected to simply take the word of a company that has earned a top spot on the list of white collar criminals; a company that in 2009 was fined a record-breaking $2.3 billion in fines for fraudulent marketing and health care fraud.9 Press releases are not science. They’re marketing. Without the raw data, we have no science upon which to base our decisions about the COVID shot.

As noted by Dr. Robert Kaplan from Stanford’s School of Medicine Clinical Excellence Research Centre, who also spoke at the meeting:

Doshi stresses how utterly unscientific a process we’re now following. He also points out that doctors have an ethical duty to not recommend a treatment for which they have no data. Quoting from a 2020 article he co-wrote:10

“The point I am trying to make is very simple,” Doshi said. “The data from COVID vaccines are not available and won’t be available for years. Yet, we are not just ‘asking’ but ‘mandating’ millions of people to take these vaccines ... Without data, it’s not science.”

Regulatory Agencies Are Designed to Fail

We’ve known the FDA is a captured agency for at least a decade. None of the issues we’re now seeing are exactly new. We’re now getting a close-up view of just how dangerous the incestuous relationship between the FDA and Big Pharma really is.

Americans are dying from COVID jab injuries at unprecedented record rates, and the FDA is completely ignoring it. Instead, it continues to push for more jabs, more injuries and more deaths. It’s complicit in causing avoidable deaths rather than protecting public health. That’s the price we’re now paying for not cleaning up the agency and sealing the revolving door between regulators and industry earlier.

In “Designed to Fail: Why Regulatory Agencies Don’t Work,”11 published in May 2012 — nearly a decade ago — William Sanjour discussed the failures of regulatory reform. He points out that the reason reforms don’t work is because they keep reforming in the wrong direction:

Sanjour points out that regulators being captured by the parties they’re supposed to regulate is far more dangerous than having no regulatory agencies at all, because “capture gives industry the power of government.” Can there be any doubt that the FDA, as an agency captured by Big Pharma in general and Pfizer in particular, now wields power over the U.S. government?

Regulatory Complexity Intentionally Hides Loopholes

Even more disturbing, Sanjour reveals that, when he was writing regulations for the EPA, he was “told on more than one occasion to make sure I put in enough loopholes. The purpose of the complexity is to hide the loopholes.” Sanjour went on to explain:

How Do We Fix It?

The question staring us in the face now is, how do we fix these regulatory agencies so that they can operate for the benefit of the public rather than private for-profit interests?

“The reason salaried government regulators can be corrupted is that writing and enforcing effective regulations is not their No. 1 priority,” Sanjour noted. “Their main objective is keeping their job and advancing their careers.” Industries, meanwhile, believe that pressuring corrupt officials is the only way to protect their business. The answer, Sanjour suggests, is:

Sanjour cites research showing that, by far, whistleblowers — who risk their jobs by speaking out — are the No. 1 fraud detection group, responsible for 19% of frauds being brought to light. The U.S. Securities and Exchange Commission, meanwhile, which exists to uncover corporate fraud, was responsible for just 7%.

So, one way we could improve the system is by issuing monetary rewards to corporate whistleblowers. “Monetary rewards for whistleblowers pay benefits far in excess of the cost when compared with hired regulatory bureaucrats,” Sanjour notes. Insurance companies can also play an important role, as they are far less likely to overlook safety shortcuts that can result in disaster. An example given by Sanjour is the BP oil spill:

A third group that makes for a far better fraud detection system than federal regulators is the public. Organizations such as Citizens for Health and Environmental Justice teaches citizens how to get involved in the enforcement of regulations, and even more can be done in that regard.

For example, the EPA could sponsor civilian testing and equip citizens living in polluted areas with resources to conduct their own testing and report back if toxic exposures are found. Sanjour continues:14

We Need to Return to the Constitution

To do any or all of that, we first need to reorganize our regulatory agencies in accordance with the U.S. Constitution. As explained by Sanjour, the U.S. has three branches of government: the legislative, executive and judicial branches. However, when regulatory agencies were formed, we diverted from this structure.

Regulations are a type of laws, and as such they should come from the legislative branch. But regulatory agencies are part of the executive branch. Judicial functions have also been usurped by regulatory agencies, and hence the executive branch.

While making changes such as those proposed by Sanjour sounds simple enough, the political pushback would be enormous, and would have to be broken through, somehow. Legally, however, it would be a reasonably simple affair.

All Congress would need to do is amend the law such that the agency administrator is stripped of its authority to write rules and implement the law. That authority would then be transferred to another agency, the administrator of which would be appointed by Congress, not the president.

“Note that these are all paper changes. They do not require any relocation, new buildings, new hires, etc. The functions all currently exist. They are merely rearranged,” Sanjour says.

At present, we can no longer overlook the FDA’s corruption. It’s costing too many lives. They have completely abandoned any semblance of working for the public good. How we get rid of them and fix the problem will become an increasingly pressing question as we move forward.

Analysis by Dr. Joseph Mercola