COVID-19
US Government ADMITS It Approved Pfizer’s COVID “Vaccine” Despite Knowing About a Long List of Trial Violations
The Vigilant Fox
The US government just admitted something shocking.
They KNEW Pfizer’s COVID “vaccine” trials were a complete sham back in 2020.
But they didn’t pursue fraud because exposing it would blow up the very health policy they’re still clinging to today.
This revelation comes from the whistleblower case of Brook Jackson, a former regional director at Ventavia, the company that ran Pfizer’s clinical trials.
In 2021, Jackson filed a lawsuit under the False Claims Act, alleging that Pfizer, Ventavia, and others committed fraud by falsifying data and violating clinical trial protocols.
And now, the government refuses to investigate further—because doing so would expose that they knowingly pushed a harmful product onto the American people.
We’ll show you the court filings with Brook Jackson in this report.
Here’s what Brook Jackson witnessed firsthand.
As regional director at Ventavia, the company running Pfizer’s vaccine trial sites, Jackson said the entire operation was riddled with serious violations. She saw falsified data, trial participants who were unblinded, staff who were poorly trained, and vaccines that were improperly stored.
Worse, she claimed the company FAILED to follow up on adverse events, including serious, potentially life-threatening ones—which recklessly endangered patients and destroyed the integrity of the entire trial.
“We were so inundated with the number of adverse events that we could not keep up,” she said. Pfizer even called asking what the plan was to handle the flood of safety reports.
She said patients weren’t even given full informed consent—her “number one concern.”
Jackson reported these issues to Ventavia. When nothing changed, she went to the FDA.
Six hours later, she was fired. The reason? “I was not a good fit,” she said. “I was not a good fit for reporting fraudulent conduct in a clinical trial.”
Jackson worked at Ventavia for just 18 days but says that’s all it took to get a grasp of the fraud she witnessed.
The court documents reveal a disturbing admission: the government KNEW about ALL the previously listed issues before granting Emergency Use Authorization for Pfizer’s COVID shot.
“The FDA was aware of the protocol violations allegedly witnessed by relator BEFORE it granted Pfizer emergency use authorization for its vaccine.”
That’s the quote from page 19 of the court documents.
The “Relator” they’re referring to is Brook Jackson.
If Jackson’s allegations were true, it would completely undermine the trial’s integrity.
So what did the FDA do with that knowledge?
According to Jackson, nothing.
“I called them. I filed a report. Did they investigate the allegations I was making? The answer is no,” she said.
In a second slap in the face to the American people, the government claimed they moved forward with the COVID shots because they had “continued access” to Pfizer’s vaccine clinical trial data.
That’s the same data the FDA tried to hide for 75 years.
Now that it’s been forced into the light, we know exactly what they were trying to cover up—data showing:
• Heart damage in young people
• A massive volume of adverse events
• Biodistribution to vital organs and dangerous accumulation
• Reproductive harm affecting fertility and pregnancy outcomes
• Deaths and severe injuries linked directly to the shot
• COVID-19 listed as a side effect
• Complete failure to stop transmission
• And much, much more.
They had access to it all. And they pushed the shots anyway.
The most disturbing admission of all comes in the third point of the case.
The court filing states:
“The government further explained that discovery and litigation obligations associated with the case would place significant burdens on FDA, HHS, and the Department of Justice and that the government should not be required to bear such burdens on a case ‘inconsistent with its health policy.’”
In plain English: the government didn’t want to investigate Pfizer, not because the fraud claims lacked merit, but because digging deeper would conflict with its official narrative that the COVID shots are “effective.”
That’s the health policy they’re clinging to.
And they’d rather bury anything that threatens to expose flaws, fraud, or harm from these shots than face the fallout of their own actions.
Jackson emphasized that her lawsuit is about one thing: fraud.
She questioned how exposing fraud could possibly go against public health policy, especially when that policy has never even been clearly defined.
“These were our taxpayer dollars used to fund their experiments,” Jackson said, adding, “these [COVID shots] are not safe or effective products. They’re contaminated, they’re dangerous, and they need to be stopped immediately.”
She called for a full recall, congressional investigations, and accountability for the dangerous experiment that’s been carried out on the American people.
“Fraud should not be allowed to be a part of a clinical trial. Period.”
Thanks for reading.
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Watch the full conversation with Brook Jackson and Maria Zeee below.
COVID-19
Trump DOJ seeks to quash Pfizer whistleblower’s lawsuit over COVID shots
From LifeSiteNews
The Justice Department attorney did not mention the Trump FDA’s recent admission linking the COVID shots to at least 10 child deaths so far.
The Trump Department of Justice (DOJ) is attempting to dismiss a whistleblower case against Pfizer over its COVID-19 shots, even as the Trump Food & Drug Administration (FDA) is beginning to admit their culpability in children’ s deaths.
As previously covered by LifeSiteNews, in 2021 the BMJ published a report on insider information from a former regional director of the medical research company Ventavia, which Pfizer hired in 2020 to conduct research for the company’s mRNA-based COVID-19 shot.
The regional director, Brook Jackson, sent BMJ “dozens of internal company documents, photos, audio recordings, and emails,” which “revealed a host of poor clinical trial research practices occurring at Ventavia that could impact data integrity and patient safety […] We also discovered that, despite receiving a direct complaint about these problems over a year ago, the FDA did not inspect Ventavia’s trial sites.”
According to the report, Ventavia “falsified data, unblinded patients, employed inadequately trained vaccinators, and was slow to follow up on adverse events reported in Pfizer’s pivotal phase III trial.” Overwhelmed by numerous problems with the trial data, Jackson filed an official complaint with the FDA.
Jackson was fired the same day, and Ventavia later claimed that Jackson did not work on the Pfizer COVID-19 shot trial; but Jackson produced documents proving she had been invited to the Pfizer trial team and given access codes to software relating to the trial. Jackson filed a lawsuit against Pfizer for violating the federal False Claims Act and other regulations in January 2021, which was sealed until February 2022. That case has been ongoing ever since.
Last August, U.S. District Judge Michael Truncale dismissed most of Jackson’s claims with prejudice, meaning they could not be refiled. Jackson challenged the decision, but the Trump DOJ has argued in court to uphold it, Just the News reports, with DOJ attorney Nicole Smith arguing that the case concerns preserving the government’s unfettered power to dismiss whistleblower cases.
The rationale echoes a recurring trend in DOJ strategy that Politico described in May as “preserving executive power and preventing courts from second-guessing agency decisions,” even in cases that involve “backing policies favored by Democrats.”
Jackson’s attorney Warner Mendenhall responded that the administration “really sort of made our case for us” in effectively admitting that DOJ is taking the Fair Claims Act’s “good cause” standard for state intervention to mean “mere desire to dismiss,” which infringes on his client’s “First Amendment right to access the courts, to vindicate what she learned.”
Mendenhall added that in a refiled case, Jackson “may be able to bring a very different case along the same lines, but with the additional information” to prove fraud, whereas rejection would send the message that “if fraud involves government complicity, don’t bother reporting it.”
That additional information would presumably include the FDA’s recent admission that at least 10 children the agency has reviewed so far “died after and because of receiving COVID-19 vaccination.”
“The truth is we do not know if we saved lives on balance,” admitted FDA Chief Medical Officer Vinay Prasad in a recent leaked email. “It is horrifying to consider that the U.S. vaccine regulation, including our actions, may have harmed more children than we saved. This requires humility and introspection.”
The COVID shots have been highly controversial ever since the first Trump administration’s Operation Warp Speed initiative prepared and released them in a fraction of the time any previous vaccine had ever been developed and tested. As LifeSiteNews has extensively covered, a large body of evidence has steadily accumulated over the past five years indicating that the COVID jabs failed to prevent transmission and, more importantly, carried severe risks of their own.
Ever since, many have intently watched and hotly debated what President Donald Trump would do about the situation upon his return to office. Though he never backed mandates like former President Joe Biden did, for years Trump refused to disavow the shots to the chagrin of his base, seeing Operation Warp Speed as one of his crowning achievements. At the same time, during his latest run he embraced the “Make America Healthy Again” movement and its suspicion of the medical establishment more broadly.
So far, Trump’s second administration has rolled back several recommendations for the shots but not yet pulled them from the market, despite hiring several vocal critics of the COVID establishment and putting the Department of Health & Human Services under the leadership of America’s most prominent anti-vaccine advocate, Robert F. Kennedy Jr. Most recently, the administration has settled on leaving the current jabs optional but not supporting work to develop successors.
In a July interview, FDA Commissioner Marty Makary asked for patience from those unsatisfied by the administration’s handling of the shots, insisting more time was needed for comprehensive trials to get more definitive data.
COVID-19
Canadian Health Department funds study to determine effects of COVID lockdowns on children
From LifeSiteNews
The commissioned study will assess the impact on kids’ mental well-being of COVID lockdowns and ‘remote’ school classes that banned outdoor play and in-person learning.
Canada’s Department of Health has commissioned research to study the impact of outdoor play on kids’ mental well-being in light of COVID lockdowns and “remote” school classes that, for a time, banned outdoor play and in-person learning throughout most of the nation.
In a notice to consultants titled “Systematic Literature Reviews And Meta Analyses Supporting Two Projects On Children’s Health And Covid-19,” the Department of Health admitted that “Exposure to green space has been consistently associated with protective effects on children’s physical and mental health.”
A final report, which is due in 2026, will provide “Health Canada with a comprehensive assessment of current evidence, identify key knowledge gaps and inform surveillance and policy planning for future pandemics and other public health emergencies.”
Bruce Squires, president of McMaster Children’s Hospital of Hamilton, Ontario, noted in 2022 that “Canada’s children and youth have borne the brunt” of COVID lockdowns.
From about March 2020 to mid-2022, most of Canada was under various COVID-19 mandates and lockdowns, including mask mandates, at the local, provincial, and federal levels. Schools were shut down, parks were closed, and most kids’ sports were cancelled.
Mandatory facemask polices were common in Canada and all over the world for years during the COVID crisis despite over 170 studies showing they were not effective in stopping the spread of COVID and were, in fact, harmful, especially to children.
In October 2021, then-Prime Minister Justin Trudeau announced unprecedented COVID-19 jab mandates for all federal workers and those in the transportation sector, saying the un-jabbed would no longer be able to travel by air, boat, or train, both domestically and internationally.
As reported by LifeSiteNews, a new report released by the Justice Centre for Constitutional Freedoms (JCCF) raised alarm bells over the “harms caused” by COVID-19 lockdowns and injections imposed by various levels of government as well as a rise in unexplained deaths and bloated COVID-19 death statistics.
Indeed, a recent study showed that COVID masking policies left children less able to differentiate people’s emotions behind facial expressions.
COVID vaccine mandates and lockdowns, which came from provincial governments with the support of the federal government, split Canadian society.
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