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Pfizer documents challenge Health Canada COVID-19 vaccine narrative

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From the Frontier Centre for Public Policy

By Ray McGinnis

Dr. Theresa Tam and senior federal health officials walked onto a stage this fall, socially distanced. Each wore masks, addressing an empty room.

Have they been living in a bubble?

The New York Times reported on February 21, 2023, that wearing masks did nothing to protect people from the COVID-19 virus.

Reporting on a rigorous and extensive study, Oxford epidemiologist Tom Jefferson said, “There is just no evidence that they [masks] make any difference. Full stop.” Jefferson said that even if one were to don an N-95 mask that it “makes no difference – none of it.” The microscopic hole in an N-95 mask was 35 microns. The much smaller droplet from the C-19 virus was 0.15 microns and could easily float through the N-19 mask hole. And why would a mask only be needed to protect us in public when we are not eating or drinking?

Health Canada continues to encourage the public to get COVID-19 boosters this fall. The agency asserts: “It’s considered safe to get both your COVID booster and a flu shot at the same appointment.” They are also “reviewing updated booster shots for children six months and up.”

However, release of the Pfizer Documents reveals people would be wise to avoid getting anymore boosters.

During its brief clinical trials, and in the first 12 weeks of the mRNA vaccine rollout, Pfizer compiled over 55,000 documents that related to clinical trials and other research the company conducted.  The company hoped these documents would be sealed from public view for 75 years.  The U.S. Food and Drug Administration supported keeping the data secret.

Nevertheless, a US court disagreed. The documents began being released in 2022. Steve K. Bannon hosted whistleblower Dr. Naomi Wolf on his War Room podcast. Together, they issued a call for medical and scientific experts to examine the documents. Project manager, Amy Kelly divided 3,500 highly trained specialists into teams. And they went through the material with a fine-toothed comb Their findings are published in the War Room/DailyClout Pfizer Documents Analysis Reports.

The teams learned that Pfizer had many reports of serious adverse events after the initial 12-week rollout – 158,000 – that they had to hire an additional 2,400 full-time staff to manage the caseload.

A Pfizer Safety Branch  Report concluded that by February 28, 2021, 1,223 people had died because of the vaccine.

Pfizer did not disclose all of its vaccine ingredients. In fact, a  news story reports: “Health Canada Confirms Undisclosed Presence of DNA Sequence in Pfizer Shot.” The Epoch Times explains that the Simian Virus 40 DNA sequence is in some of the the Pfizer mRNA vaccine, citing scientists who warn that it can be carcinogenic.

It seems that Pfizer kept sloppy records of the clinical trials. Pfizer Documents Investigation Team 5 reported: “a great deal of data… [is] missing from Pfizer’s analysis of adverse events that were reported after the Pfizer mRNA vaccine was approved by the US Food and Drug Administration…. The outcomes of almost one-quarter (22%) are not known.” They added, “Pfizer’s 3.7% fatality rate for the adverse event cases with known outcomes doesn’t include patients that Pfizer said had not recovered at the time of the report (30 April 2021).”

Team 1 reported that from December 1, 2020, “Pfizer was aware that the vaccine…had limited efficacy.” They reported that:“1,625 serious cases of vaccine ineffectiveness….” This included 136 people dying of COVID-19 related pneumonia after getting the Pfizer shot.

Team 3 examined what Pfizer did to ensure the safety of their vaccine. Did the vaccine stay in the arm, or did it travel to other places?

It was known that the engineered nanomaterials in the vaccine can cross or bypass the blood-brain barrier. What were the implications for the central nervous system? Team 3 discovered that: “This evaluation was never done in the Pfizer safety and efficacy trials… it is impossible to know whether the vaccine is safe in this arena. Pfizer did not prove the safety of the nano-lipid delivery system for the brain:” They just didn’t look under that rock.

In March 2022, the Journal of Pediatrics reported that the Seattle Children’s Hospital at the University of Washington had 35 cases of myocarditis in children within one week of receiving the second dose of the Pfizer vaccine. Team 1 reported that it was clear to both Pfizer and the FDA that by June 2021 there was a “serious problem of myocarditis in adolescents following mRNA vaccination….” Nonetheless, the FDA went ahead and issued the Emergency Use Authorization to include teenagers, and they did not mention the risks.

The Pfizer Documents also reveal that by February 28, 2021, they knew that serious stroke adverse events were occurring after vaccination. Pfizer observed 275 patients who had a stroke post-vaccine….“Strokes are life-altering events. Even Pfizer categorized all the reported stroke as serious.” Nonetheless, even after Pfizer examined the stroke adverse events, they offered an upbeat assessment: “This cumulative case review does not raise new safety issues.”

And what did Health Canada say?

Journalist Rodney Palmer reported to the National Citizens Inquiry that the Government of Canada reported that by “March 3, 2023, [there were] a total of 427 reports with an outcome of death…reported following vaccination.”

Unfortunately, Canadians are still living in a bubble with little understanding of the adverse effects of the COVID-19 vaccines and boosters.

 

Ray McGinnis is a senior fellow at the Frontier Centre for Public Policy, and author of Unanswered Questions and Writing the Sacred.

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COVID-19

Trump DOJ seeks to quash Pfizer whistleblower’s lawsuit over COVID shots

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From LifeSiteNews

By Calvin Freiburger

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.”

“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.

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COVID-19

University of Colorado will pay $10 million to staff, students for trying to force them to take COVID shots

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From LifeSiteNews

By Calvin Freiburger

The University of Colorado Anschutz School of Medicine caused ‘life-altering damage’ to Catholics and other religious groups by denying them exemptions to its COVID shot mandate, and now the school must pay a hefty settlement.

The University of Colorado’s Anschutz School of Medicine must pay more than $10.3 million to 18 plaintiffs it attempted to force into taking COVID-19 shots despite religious objections, in a settlement announced by the religious liberty law firm the Thomas More Society.

As previously covered by LifeSiteNews, in April 2021, the University of Colorado (UC) announced its requirement that all staff and students receive COVID jabs, leaving specific policy details to individual campuses. On September 1, 2021, it enforced an updated policy stating that “religious exemption may be submitted based on a person’s religious belief whose teachings are opposed to all immunizations,” but required not only a written explanation why one’s “sincerely held religious belief, practice of observance prevents them” from taking the jabs, but also whether they “had an influenza or other vaccine in the past.”

On September 24, the policy was revised to stating that “religious accommodation may be granted based on an employee’s religious beliefs,” but “will not be granted if the accommodation would unduly burden the health and safety of other Individuals, patients, or the campus community.”

In practice, the school denied religious exemptions to Catholic, Buddhist, Eastern Orthodox, Evangelical, Protestant, and other applicants, most represented by Thomas More in a lawsuit contending that administrators “rejected any application for a religious exemption unless an applicant could convince the Administration that her religion ‘teaches (them) and all other adherents that immunizations are forbidden under all circumstances.’”

The UC system dropped the mandate in May 2023, but the harm had been done to those denied exemptions while it was in effect, including unpaid leave, eventual firing, being forced into remote work, and pay cuts.

In May 2024, a three-judge panel of the U.S. Tenth Circuit Court of Appeals rebuked the school for denying the accommodations. Writing for the majority, Judge Allison Eid found that a “government employer may not punish some employees, but not others, for the same activity, due only to differences in the employee’s religious beliefs.”

Now, Thomas More announces that year-long settlement negotiations have finally secured the aforementioned hefty settlement for their clients, covering damages, tuition costs, and attorney’s fees. It also ensured the UC will agree to allow and consider religious accommodation requests on an equal basis to medical exemption requests and abstain from probing the validity of applicants’ religious beliefs in the future.

“No amount of compensation or course-correction can make up for the life-altering damage Chancellor Elliman and Anschutz inflicted on the plaintiffs and so many others throughout this case, who felt forced to succumb to a manifestly irrational mandate,” declared senior Thomas More attorney Michael McHale. “At great, and sometimes career-ending, costs, our heroic clients fought for the First Amendment freedoms of all Americans who were put to the unconscionable choice of their livelihoods or their faith during what Justice Gorsuch has rightly declared one of ‘the greatest intrusion[s] on civil liberties in the peacetime history of this country.’ We are confident our clients’ long-overdue victory indeed confirms, despite the tyrannical efforts of many, that our shared constitutional right to religious liberty endures.”

On top of the numerous serious adverse medical events that have been linked to the COVID shots and their demonstrated ineffectiveness at reducing symptoms or transmission of the virus, many religious and pro-life Americans also object to the shots on moral grounds, due to the ethics of how they were developed.

Catholic World Report notes that similarly large sums have been won in other high-profile lawsuits against COVID shot mandates, including $10.3 million to more than 500 NorthShore University HealthSystem employees in 2022 and $12.7 million to a Catholic Michigander fired by Blue Cross Blue Shield in 2024.

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