Health Canada won’t answer contaminated COVID-19 vaccine questions

This month Ottawa tabled a stack of Order Paper Questions on COVID vaccines: Pfizer payments, residual DNA contamination known as Plasmidgate, approvals, VAERS death reports, and the science (or lack thereof) behind lockdowns.

As then Prime Minister Justin Trudeau sold vaccination as a civic duty and implemented sweeping vaccine mandates, families who were never given proper informed consent recently brought their injuries to Ottawa.

“It really affects the whole family when one person’s injured,” said Carrie Sakamoto, a severely vaccine injured Canadian. She told me at the Allison Inquiry at the beginning of September that “it just devastates everybody.”

Veterans, former elite athletes and parents of children who died testified, and Health Canada stayed silent throughout. Then, a week later, the Public Health Agency of Canada posted a portal update and a backlog number. There was no apology.

As OPQ responses begin rolling in, one is from the MP who spearheaded the inquiry, Dean Allison himself. He asked Health Canada what science proves SV40 promoter fragments in Pfizer’s vaccine are inactive, and when officials first noticed the 2021-22 spike in U.S. VAERS death reports.

The department responded not with a study, but the blanket reassurance that the fragment is inactive, has no functional role and sits below limits. For context: SV40 sequences are used in molecular biology to drive gene expression. They can interact with host DNA, but it all begs the question that if the material is inert and irrelevant, why is it there?

Internal Health Canada emails from July 2023 show officials still asking Pfizer for characterization details while authorizing additional boosters – shots that were still contaminated.

Pfizer had not disclosed the sequence to Health Canada, the FDA or the EMA at the time of submissions, and it was only after genomics expert Kevin McKernan and I made the finding public in April, agencies compared notes.

“At Health Canada, we do not view this as an urgent risk topic,” one email said, as fall booster campaigns loomed. If regulators had already concluded the fragment was harmless and below limit, why were they still seeking basic measurement information from Pifzer?

The same pattern appears in questions on residual DNA bound to lipid nanoparticles, the tiny fat bubbles that carry the modified RNA of the vaccine into cells.

Officials once again offered broad safety assurances while leaving levels, fragment size, batch variability and manufacturing controls unanswered. On deaths, they said vital statistics showed no increase linked to mRNA vaccines, cited VAERS when convenient, then treated the same database as a scare tactic.

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COVID mRNA Vaccine Hides Up to 30% of Endotoxin Activity in FDA Test

All FDA-approved and emergency-use-authorized mRNA vaccines use E. coli to produce so-called starting DNA or other manufacturing materials, creating a lipopolysaccharide (LPS) endotoxin contamination risk that manufacturers test for in the finished shots.

Endotoxin has been shown to drive cardiac injury and abnormal clotting in experimental studies, and other outcomes that overlap with myocarditis, blood clots, and other serious events reported after Pfizer’s COVID-19 mRNA vaccine, raising the question of whether endotoxin was adequately excluded as a contributor.

No publicly available information tells us specifically how much endotoxin is present in finished mRNA vaccine vials.

In a January 2022 memo, the FDA reported adding a known amount of endotoxin to three samples of Moderna’s finished COVID vaccine to check whether its test could detect it.

Its test only recovered 80%, 71%, and 70% of the added activity.

Meaning 20%, 29%, and 30% of the control signal went undetected while the added endotoxin was present in the samples.

The endotoxin was still there.

FDA knew how much it had added.

Yet something in the vaccine samples prevented the test from detecting up to 30% of its activity.

FDA nevertheless accepted all three results, raising questions:

  • If the test missed up to 30% of a control added after manufacture, what could it miss when endotoxin enters the vaccine’s lipid particles during manufacture?
  • Why did FDA call the measured loss only “slight inhibition”?
  • And why did the agency allow a complete finished-product release test to wait until after its Spikevax approval decision?
  • Why have regulators and manufacturers not told us exactly how much LPS endotoxin is present in finished mRNA vaccine vials?
  • Why do post-mRNA vaccination adverse events track endotoxin exposure symptoms?

Australian regulator TGA did test Pfizer’s mRNA COVID vaccine batches as “less than 5 EU/mL.”

But that means the assay couldn’t see endotoxin above a prespecified cutoff, and only after it was diluted.

It is not a count of how much total endotoxin is in each vial.

Moreover, studies examined below found that liposomes and other lipid preparations can hide over 90% of incorporated endotoxin from detection, raising the question of what happens in the lipid nanoparticles used in mRNA vaccines.

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In Shadow of Pending Lawsuit, CDC Again Recommends COVID Vaccines for Infants and Young Kids

The Centers for Disease Control and Prevention (CDC) quietly reinstated its July 2025 COVID-19 vaccination recommendations, including recommending the vaccine for “off-label” use among infants and children, Maryanne Demasi, Ph.D., reported.

According to the CDC’s updated webpage, the agency now recommends the COVID-19 shot for all adults ages 18 and older and for children ages 6 months to 17 years who are moderately to severely immunocompromised.

For children not at high risk — including males ages 12-24, who have the highest risk for vaccine-associated myocarditis — the CDC recommends the vaccine based on shared clinical decision-making.

The updated recommendations conflict with U.S. Food and Drug Administration (FDA) approvals for the vaccines.

There are currently no FDA-approved COVID-19 vaccines for healthy children and adults younger than 64. For those younger than 65, the vaccines are only FDA-approved for those at high risk of COVID-19 illness, at various ages depending on the vaccine.

The CDC acknowledges that use of the vaccine in that age group would be an “off-label” use.

Latest changes may be tied to court order in ongoing lawsuit

In May 2025, the U.S. Health Secretary Robert F. Kennedy Jr. announced that the CDC would no longer recommend COVID-19 vaccines for healthy children 6 months and older and healthy pregnant women.

In September 2025, the CDC Advisory Committee on Immunization Practices (ACIP) made the changes official when members voted that for people ages 6 months to 64 years, COVID-19 vaccination should be based on “individual-based decision-making.”

However, a court-ordered stay in March 2026 froze those recommendations. To comply with that order, the CDC is now reverting to its early 2025 recommendations.

The court-ordered stay, issued by U.S. District Judge Brian E. Murphy, stemmed from an ongoing lawsuit filed in July 2025 by the American Academy of Pediatrics (AAP) and several other medical groups.

The groups sued Kennedy and the U.S. Department of Health and Human Services (HHS) over changes to COVID-19 vaccine recommendations for children and pregnant women. They amended their lawsuit several times in response to new HHS and CDC policies and recommendations.

The U.S. Department of Justice is appealing Murphy’s ruling on behalf of Kennedy and HHS. Oral arguments are scheduled for Oct. 6 before the U.S. Court of Appeals for the 1st Circuit.

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FDA Commissioner Nominee Says Every Vaccine On US Market Is Safe, Effective

The doctor nominated by President Trump to lead the Food and Drug Administration (FDA) told senators this week that vaccines available in the United States are safe and effective.

Dr. Heidi Overton, the nominee, said that if confirmed, she could use her scientific training and clinical background to describe to the American public what is currently known about products that fall under Food and Drug Administration oversight.

“And what is currently known is that the vaccines that have been approved by the FDA meet the standards for safety and efficacy,” she said.

Overton, 37, also endorsed the measles, mumps, and rubella vaccine, saying it is not lethal and that it is the best tool in the public health response to measles outbreaks that are ongoing in the United States.

She said that mifepristone, an abortion pill, was safe and effective because it had been approved by the FDA. Overton wrote in a 2023 article that chemical abortion through products such as mifepristone was “dangerous to women,” drawing criticism from Democrats in the Senate.

As Zachary Stieber reports further for The Epoch Times, Overton would take the helm of an agency that has been under acting leadership since Dr. Marty Makary stepped down in May.

While signing an executive order in August that encouraged breaking up the measles combination vaccine, Trump told reporters that the vaccine is possibly “quite lethal” and that separate shots for measles, mumps, and rubella appeared to be “not at all lethal but just very effective.”

When asked after the signing, the White House declined to provide any citations for Trump’s description of the vaccine.

Leaders in the Make America Healthy Again movement recently called for removing vaccines containing messenger ribonucleic acid (mRNA) technology.

Sen. Bill Cassidy (R-La.), an outspoken vaccine proponent, has been asking people whom Trump nominated to serve in high-level health positions about Trump’s comments, as well as other questions about vaccines, during their confirmation hearings before the Senate Health Committee, the panel he chairs. Chris Klomp, selected to be the top deputy to Health Secretary Robert F. Kennedy Jr., recently voiced support for vaccines in response to Cassidy, as did Dr. Nicole Saphier, tabbed to become surgeon general.

Cassidy said on Sept. 24 that Kennedy, whom he voted for, made him guarantees but later backtracked on those promises, citing directives from the president.

Kennedy’s department did not return a request for comment.

Cassidy asked Overton how she would handle it if she made guarantees and the president then directed her to go against them.

“I’ve had robust discussions with the president,” said Overton, who was part of Trump’s first administration.

“I would give him my best advice, and I would follow the statutory requirements for the role of FDA commissioner regarding individual product determinations for safety and efficacy, and that would be what would guide every decision if confirmed to this role.”

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Vaccines have never been safe and effective: A century of documented failures of smallpox vaccination

“At one time it was believed and generally understood that after we had once had the disease we were for ever secure against it, but it is now proved that a second and even a third attack is by no means uncommon among persons of a peculiar habit of body, and whose lives are spent in opposition to all sanitary laws. This error led to that blind infatuation of being inoculated for the Small-pox which became so fashionable in the last century, and which, after much controversy, was adopted by the London College of Physicians, who considered it ‘highly beneficial to mankind’.”—William Job Collins, MD, twenty-five years public vaccinator, London, England, 1869[1]

“Millions of vaccinations are made every year, and nobody knows what they are made with. The whole process is a haphazard game with chance. Vaccination was accepted on the simple dictum of Jenner that it would stamp out smallpox. The medical profession of today buys its vaccinal virus of those who make merchandise of it on their simple dictum that it is the right thing to use … I compiled a list of upwards of a thousand instances of persons who had suffered permanent injury, or death [from vaccination] … Of these, nine have been personally known to me.”—George William Winterburn, PhD, MD, author of The Value of Vaccination: A Non-partisan Review of Its History and Results, 1886[2]

“Cow-pox was exceedingly virulent and fatal disease coming to fag end of its career in Jenner’s time. He found it difficult to get lymph from the cow, and therefore he resorted to the heels of horses; and the original lymph we use from the Royal Vaccine Institute has never been vaccine lymph at all; from the day it was introduced into London to the present time – it was derived from the arm of Jane King, who was inoculated from a horse with greasy heels.”—John Le Gay Brereton, Esq., MD, MRCS, LAC, 1881[3]

“This madness – first filtered through the brain of Jenner by the superstitious old women of Berkeley and its neighbourhood, who had long secretly practised vaccination upon children – was, after some few years of hard fighting, transmitted to Sir Gilbert Blane and a few of his class; and as these were the great ‘medicine men,’ whose wisdom excelled all others, the delusion was soon shared by the King. From the King it passed to the Court, from the Court to the Government, from the Government to the profession, and from the profession to all who readily move by example in high places. In this way, not England alone, but every part of the civilised world, more or less, went mad; and humanity is now reaping its reward – not in the extirpation of small-pox, as promised by these fanatics, but in the increase of diseases more frightful in their character, and in their general results more fatal.”— Dr. Skelton, Licentiate in Medicine and Surgery, London and Edinburgh[4]

In 1796, Edward Jenner tested a popular belief: that cowpox protected against smallpox. He obtained cowpox material from a milkmaid and used it to inoculate an eight-year-old boy named James Phipps, whom he then deliberately exposed to smallpox. Because the boy did not fall ill, Jenner concluded that the procedure – cowpoxing, later given the more scientific-sounding and mysterious name vaccination (from vacca, Latin for cow) – was effective and conferred lifelong protection. On 17 March 1802, he informed the House of Commons that vaccination was entirely safe, granted lifelong immunity and would rid the world of smallpox.[5]

From the outset, however, many regarded this new notion – built on eighty years of smallpox inoculation – as anything but safe or effective. Yet the idea took hold almost immediately. As Dr. William Rowley, MD, observed in 1805 – less than a decade since vaccination had started – “Whoever had not taken the oaths of supremacy and allegiance to vaccination, or who dared to doubt the infallibility of Cow-pox inoculation even in its infancy, even before any judgment could be formed, were ignominiously treated as traitors to the royal vaccinating state, as rebellious subjects to the Jennerian despotic power.”[6] Decades later, Dr. Charles Creighton likewise noted how firmly this idea had taken root: by 1801, he wrote, professors and others of his class “on the Continent as well as in England were already deeply committed“ and that “anyone who undertakes to answer for Jenner and his theories, must shatter his own reputation for scientific and historical knowledge.”[7]

What follows is not a history of vaccination’s triumphs but a record of its failures – drawn almost entirely from the testimony of physicians who witnessed them firsthand. The timeline that unfolds across the following decades chronicles smallpox vaccination’s inability to shield against the very disease it promised to conquer, together with the injuries and deaths that followed in its trail. The quotations assembled here, spanning 1799 to 1910, call into question the triumphant narrative so widely accepted about this medical intervention.

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Do you know why doctors and nurses remained silent about all the clots, strokes, etc. after the COVID shot rollout?

After the COVID shots rolled out, critical care units of hospitals were seeing massive spikes in clots and strokes.

Why didn’t they speak up?

Because they didn’t want to lose their job (or their medical license) for creating vaccine hesitancy.

I wish I was kidding about this, but I’m not.

I heard this directly from the nursing staff at a large hospital I was just at.

This is why people don’t trust doctors. It’s not the fault of “misinformation spreaders.” It’s because doctors aren’t allowed to tell us the truth.

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Army flight surgeon drops bombshell: 29 troop deaths after COVID shot, 55,000 adverse-events, and 2,500 death files now under review

A bombshell sworn declaration filed in federal court is raising new questions about the Biden-era COVID-19 vaccine mandate imposed on America’s military.

According to TrialSite News, Army Lt. Col. Theresa Long, a retired Army flight surgeon now serving as senior medical military adviser to Health Secretary Robert F. Kennedy Jr. and reporting to War Secretary Pete Hegseth, filed a sworn declaration in Adirim v. U.S. Central Intelligence Agency et al., in the Eastern District of Virginia.

Long told the court she has firsthand knowledge of more than 29 service-member deaths after COVID-19 vaccination and that she has been tasked with examining roughly 55,000 military-linked adverse-event reports, including 2,544 death reports in the federal Vaccine Adverse Event Reporting System (VAERS).

“I have first hand knowledge of over 29 deaths of servicemembers after vaccination with the COVID-19 vaccines. I am currently tasked with investigating the 55,000 vaccine adverse event reports filed on individuals identified as members of the U.S. Armed Forces, this includes 2544 deaths.

“As the first aviation brigade surgeon I had one servicemember die of rapid onset and progression of esophageal cancer after COVID vaccination and one in which a student pilot who had never been COVID positive, who experienced sudden cardiac death at the controls of a helicopter during a training flight.

“An independent cardiologist evaluated all imaging, labs and history on the student pilot and determined that myocardial injury secondary to the COVID-19 vaccines was the most likely cause.

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Vaccine-Injured Canadians Finally Got a Hearing. Health Canada Was Absent.

For years, vaccine-injured Canadians have described being ignored, gaslit, and left to navigate serious illness with little help or compensation. Their questions extend beyond their own medical care: Who knew about the risks? How were reports of injury investigated? And who is responsible for helping them now?

Other countries have opened their pandemic decisions to public scrutiny. According to the Allison Inquiry’s organizers, more than 30 democracies have held some form of inquiry into their pandemic response. Though those proceedings have differed in scope and conclusions, Canada has yet to hold a national public inquiry of any sort.

Conservative MP Dean Allison decided Canadians should not have to keep waiting.

With lawyer Shawn Buckley as inquiry counsel and a volunteer team behind him, Allison organized four days of hearings on Parliament Hill focused on COVID-19 vaccine injuries. More than 1,400 people applied to testify. From September 8 to 11, roughly 50 witnesses took the oath, including injured Canadians, bereaved families, physicians, and researchers.

The hearings had limited powers. They could not compel witnesses or subpoena records, and their terms prohibited findings of fact or conclusions. Even within those limits, witnesses could explain publicly what had happened to them and what they wanted investigated.

Health Canada did not testify.

CBC published a report on the final afternoon. Global News aired a segment two days after the hearings closed. The testimony itself deserves attention: families describing lives upended, physicians recounting their attempts to report injuries, and researchers questioning how those reports were handled.

IMA readers will recognize several participants, including Senior Fellow Dr. Jessica Rose, Senator Ron Johnson, and Dr. James Thorp. Below are eight witnesses and excerpts from their testimony. For those seeking help with symptoms after vaccination, IMA’s free post-vaccine treatment guide offers a resource to discuss with a treating clinician.

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FDA relied on broken data mining process to sell COVID vaccines: report

Top officials with the U.S. Food and Drug Administration (FDA) were warned in early 2021 of a critical defect in the country’s vaccine monitoring system yet chose to rely on it anyway while assuring the public of the COVID-19 vaccines’ safety, according to a new report.

On September 16, the British Medical Journal (BMJ) published a report detailing flaws in the algorithms used to sift through the federal Vaccine Adverse Event Reporting System (VAERS) to find safety signals with the COVID shots that would require investigation.

One of those algorithms would calculate “proportional reporting ratios” (PRRs), identifying events that were reported at a higher rate than others, along with “empirical bayesian” data mining.

But according to the BMJ’s investigation, the agency’s algorithm was “mathematically compromised by the deluge of covid vaccine adverse event reports – resulting in a near total loss of signal detection sensitivity for the new mRNA vaccines made by Pfizer and Moderna.” More significantly, top officials were warned early in 2021, yet chose to keep relying on it anyway, and even “cited the absence of signals when assuring clinicians and the public of the vaccines’ safety.”

In February 2021, the Israeli Ministry of Health informed the FDA and CDC of a “a large number of reports of myocarditis, particularly in young people” after vaccination, and followed up five weeks later that two of the 77 had died. The Pentagon Defense Health Agency subsequently reported a “cluster” of myocarditis cases among male soldiers. By May, VAERS had gotten hundreds of such reports, prompting the CDC to begin alerting medical professionals.

Then-FDA Center for Biologics Evaluation & Research director Peter Marks emailed CDC director Rochelle Walensky, expressing concern that “myocarditis and pericarditis have not actually signaled … Can you help me understand why we are doing this when pediatricians and others in the community already seem to be aware?”

As VAERS reports continued to mount, health officials inquired as to why they were not receiving safety signals from the government.

“The problem arose because, in the first year of the rollout, almost all the reports coming into VAERS – more than 90% of 1.1 million – were for the mRNA covid shots, dwarfing vaccines for all other diseases,” BMJ explained. “This meant that analyzing the safety of one vaccine, for example Pfizer’s product, involved comparing it to other vaccines, which were overwhelmingly limited to Moderna’s product. But if both mRNA vaccines elevated the risk of an adverse event like myocarditis in roughly equal amounts, the ‘observed’ frequency and ‘expected’ frequency would be similar, resulting in no automated alert. The statistical phenomenon is known as ‘masking.’”

Microbiologist and immunologist Ana Szarfman, an expert in drug safety data mining who worked with the FDA for decades, emailed Marks directly with concerns about the system. Two weeks later, a video conference was held in which Szarfman’s presentation explained that the PRR analysis “Highlights almost everything,” whereas the FDA’s bayesian approach did not: “You are not getting useful information with such low counts.”

Yet Marks and his team declined to change course and urged Szarfman to “hold off on creating and sending data mining reports and analyses using covid-19 vaccine AE (adverse event) data.”

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Anthrax Attacks Paved Way for COVID-Era ‘Junk Drugs and Vaccines’

The anthrax attacks that followed 9/11 did more than frighten Americans — they helped create the legal, regulatory and biosecurity framework that later enabled the government’s response to COVID-19, according to Dr. Meryl Nass.

Speaking at the Turning the Tide: 9/11 25 Years Later conference last week in New York City, Nass drew a direct line between the anthrax letters of 2001 and the coronavirus pandemic.

“It’s worth thinking about the similarities between the COVID experience and the anthrax letters because it seems that both were inside jobs planned by the same cabal for the same purpose,” Nass said.

Nass, an internal medicine physician who has conducted extensive research on biological warfare and anthrax, outlined what she sees as striking parallels between the two events.

“Each had an uncanny, scripted simulation preceding it,” she said, pointing to the Dark Winter tabletop exercise in 2001 and Event 201, a pandemic simulation, in 2019.

“Each was blamed on countries the U.S. government had already targeted,” Nass said. The anthrax attacks were initially blamed on Iraq while COVID-19 was blamed on China.

“A huge, expensive biodefense gravy train resulted after each of them,” she said.

Both events were also accompanied by “a massive amount of false narrative construction and control of the media to project the false narratives.” And neither received a serious investigation into who perpetrated the event, according to Nass.

In addition, both crises “led to a mushrooming of the surveillance state,” Nass said.

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