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‘We need to ask these questions’: Experts accuse government, Pharma of covering up vaccine risks

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From LifeSiteNews

By Michael Nevradakis Ph. D., The Defender

Medical experts, political figures, journalists and whistleblowers today accused public health agencies and the mainstream media of censoring and covering up information relating to COVID-19 vaccine injuries and adverse events during a U.S. Senate roundtable discussion.

Sen. Ron Johnson hosted the discussion – “Federal Health Agencies and the COVID Cartel: What Are They Hiding?” – which his office said was intended to “expose the truth about how the COVID cartel – federal health agencies, Big Pharma, legacy media, and Big Tech – engaged in censorship and coverups.”

“It was heartening to hear these courageous experts willing to risk careers and reputations in order to tell the truth despite tremendous pressure to look the other way,” said Laura Bono, Children’s Health Defense (CHD) vice president.

Bono, who attended the roundtable, added:

We can’t ensure that the global devastation caused by the COVID crisis will never occur again unless we are able to analyze what happened and speak about it freely. We are immensely grateful to Senator Johnson for presenting this crucial discussion to the American public.

The discussion focused on six topics: COVID-19 vaccine issues, the history of vaccine injury cover-ups, the corruption of medical research and federal public health agencies, media censorship and propaganda, the COVID-19 response in other countries and the World Health Organization’s (WHO) proposed “pandemic agreement.”

Brian Hooker, Ph.D., CHD chief scientific officer, told The Defender he was “riveted listening to the panelists during the entire four-hour session.”

Hooker, co-author with Robert F. Kennedy Jr. of Vax-Unvax: Let the Science Speak, participated in the roundtable, highlighting the health risks posed by vaccines and the lack of adequate testing by federal health agencies.

HHS never submitted required vaccine safety report to Congress

In his testimony, Hooker said, “The CDC [Centers for Disease Control and Prevention] has never tested the cumulative effect of the vaccine schedule on childhood health outcomes.”

He referenced several scientific studies to support his testimony.

Vaccinated children were at least twice as likely to be diagnosed with developmental delays, ear infections and gastrointestinal disorders. The likelihood of an asthma diagnosis among the vaccinated group was four-and-a-half times higher than the unvaccinated group,” he said.

Hooker said unvaccinated children have shown “incidence rates between 4-20 times lower” than vaccinated children for autoimmune, neurodevelopmental and other disorders.

He also referred to the sharp rise in myocarditis diagnoses following COVID-19 vaccination.

“Myocarditis is a serious disorder and 76% of all cases following COVID-19 vaccination, as reported to the Vaccine Adverse Event Reporting System [VAERS], required emergency care and/or hospitalization,” he said. Yet, the “CDC significantly downplays myocarditis as a side effect of the vaccine.”

Further highlighting government inaction in studying and responding to vaccine injuries, Hooker said:

The 1986 National Childhood Vaccine Injury Act requires that the Department of Health and Human Services (HHS) report to Congress on the state of vaccine safety in the U.S. every two years.

Yet HHS has “never submitted a vaccine safety report to Congress,” he said.

Big Pharma ‘controls the levers of power,’ suppresses unprofitable treatments

Edward Dowd, a former BlackRock executive who has extensively studied the increase in excess deaths during and after the COVID-19 pandemic, also participated in the roundtable.

Dowd, author of Cause Unknown’: The Epidemic of Sudden Deaths in 2021 and 2022, said that government and WHO statements claiming the COVID-19 vaccines were “safe and effective” have “been proven false.”

“It has become clear that the U.S. government, along with the health regulators, do not desire an honest accounting of … policies that were imposed mostly under federal mandates,” he said, noting that this has resulted in high human costs.

Dowd told the panel:

The total excess deaths since the rollout of the vaccine in the U.S. is approximately 1.1 million for 2021, 2022 and 2023. We estimate the economic cost of productive working age people dying at $15.6 billion [and] estimate 28.4 million individuals are chronically absent, resulting in an estimated economic cost of $135 billion since 2021.

Jessica Rose, Ph.D., an immunologist and biochemist, told The Defender in advance that her testimony would focus on an “Analysis of the VAERS pharmacovigilance database in the context of the COVID-19 injectable products,” which “has revealed strong emergent safety signals – from myocarditis to death – that are not being acknowledged by the owners of the data.”

“This goes against standard operating procedures and begs the question: Why?” she said.

Rose also referred to recent revelations, later confirmed by Canadian public health authorities, about the contamination of COVID-19 mRNA vaccines.

“Is there a risk associated with DNA insertion in the context of the modified mRNA shots? Yes,” she said.

Dr. Pierre Kory, president and chief medical officer of the Frontline COVID-19 Critical Care Alliance, discussed the suppression of potentially effective treatments by public health agencies.

“We are only now beginning to understand that many long-established drugs may have other uses that we don’t even know about, effectively treating diseases we never imagined using them against,” he said. “So why on earth aren’t we systematically testing them for potential new uses?”

Kory told the panel:

The ugly truth is it’s not profitable. Big Pharma makes money on complicated new drugs, and it controls the levers of power. Nearly half of FDA’s [U.S. Food and Drug Administration] budget is bankrolled by the drug industry, and its tentacles are deep in academia, medicine and other regulatory agencies like the NIH [National Institutes of Health].

He cited ivermectin and hydroxychloroquine as examples of treatments that were suppressed during the pandemic despite evidence they were effective.

 

Johnson: Those who ask questions ‘vilified,’ ‘ridiculed’

In an interview with The Gateway Pundit Sunday, Johnson discussed adverse events related to the COVID-19 vaccines, the discovery by embalmers of “strange white fibrous clots” in bodies of the deceased since the vaccine rollout began in late 2020 and efforts to suppress ivermectin and hydroxychloroquine as COVID-19 treatments.

Referring to the clotting phenomenon, Johnson said, “What’s unfortunate is the medical establishment in general, and certainly, our federal health agencies, are discouraging autopsies. So, the only evidence we’re getting of this is from embalmers that are having a difficult time getting embalming fluid into [the] cadavers.”

Johnson suggested that Big Pharma and government health agencies promoted mRNA vaccines because of a profit motive.

He said:

They’ve had this mRNA platform. It never succeeded in animals, but they knew how profitable a platform it could be. They’ve already found out how profitable vaccines are because there’s no worry of liability. You just get those things on the childhood vaccine schedule, and you just start printing money.

Nobody can question the efficacy. Nobody can question the safety of them. So, vaccines are highly profitable for pharmaceutical companies, so they’re going to push them. And of course, they’ve got their individuals in government that push them right along with them.

Again, our health agencies have been completely captured by Big Pharma.

Johnson also questioned the addition of an increasing number of vaccines to the childhood vaccination schedule in the U.S.

“With the number [of vaccines] we administer to children now, gee, what could go wrong?” he said. “Every time you inject a child with a vaccine, you’re messing with their immune system. Is that why autoimmune diseases are up?”

“We need to ask these questions,” Johnson said. “My problem is we’re just not even able to ask questions, and those who ask questions, those who put forward evidence are immediately ostracized, criticized, vilified, ridiculed – and that’s not science.”

Johnson also implied that some of his congressional colleagues have sustained injuries related to the COVID-19 vaccines but are not speaking out.

“My guess is they understand how people that do question this stuff are ridiculed and vilified. And they just don’t want to put up with the hassle,” he said.

Johnson also spoke out against pharmaceutical company advertising, suggesting it should be subject to a government ban.

“Pass a law,” he said. “We are one of the very few countries that allow that.”

Johnson said that while he is “a free-market guy” who usually “would not be on the side of imposing that kind of government restriction on business,” he said that having seen how Big Pharma “spends the billions and how they use that to capture the narrative and destroy anybody who questions the narrative,” he believes “that’s got to stop.”

Participants at the roundtable included:

Several of the participants – and Sen. Johnson – previously spoke at this past weekend’s International Crisis Summit in Washington, D.C., which Malone organized. Rep. Greene recently spoke in support of vaccine injury victims at a U.S. House of Representatives vaccine safety hearing.

Watch Sen. Johnson’s roundtable discussion here:

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

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COVID-19

Study finds Pfizer COVID vaccine poses 37% greater mortality risk than Moderna

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From LifeSiteNews

By Nicolas Hulscher, MPH

A study of 1.47 million Florida adults by MIT’s Retsef Levi and Surgeon General Joseph Ladapo finds significantly higher all-cause mortality after Pfizer vaccination compared to Moderna

A new study of 1.47 million Florida adults by MIT’s Retsef Levi and Surgeon General Joseph Ladapo finds significantly higher all-cause, cardiovascular, and COVID-19 mortality after Pfizer vaccination.

The study titled “Twelve-Month All-Cause Mortality after Initial COVID-19 Vaccination with Pfizer-BioNTech or mRNA-1273 among Adults Living in Florida” was just uploaded to the MedRxiv preprint server. This study was headed by MIT Professor Retsef Levi, with Florida Surgeon General Dr. Joseph Ladapo serving as senior author:

Study Overview

  • Population: 1,470,100 noninstitutionalized Florida adults (735,050 Pfizer recipients and 735,050 Moderna recipients).
  • Intervention: Two doses of either:
    • BNT162b2 (Pfizer-BioNTech)
    • mRNA-1273 (Moderna)
  • Follow-up Duration: 12 months after second dose.
  • Comparison: Head-to-head between Pfizer vs. Moderna recipients.
  • Main Outcomes:
    • All-cause mortality
    • Cardiovascular mortality
    • COVID-19 mortality
    • Non-COVID-19 mortality

All-cause mortality

Pfizer recipients had a significantly higher 12-month all-cause death rate than Moderna recipients — about 37% higher risk.

  • Pfizer Risk: 847.2 deaths per 100,000 people
  • Moderna Risk: 617.9 deaths per 100,000 people
  • Risk Difference:
    ➔ +229.2 deaths per 100,000 (Pfizer excess)
  • Risk Ratio (RR):
    ➔ 1.37 (i.e., 37% higher mortality risk with Pfizer)
  • Odds Ratio (Adjusted):
    ➔ 1.384 (95% CI: 1.331–1.439)

Cardiovascular mortality

Pfizer recipients had a 53% higher risk of dying from cardiovascular causes compared to Moderna recipients.

  • Pfizer Risk: 248.7 deaths per 100,000 people
  • Moderna Risk: 162.4 deaths per 100,000 people
  • Risk Difference:
    ➔ +86.3 deaths per 100,000 (Pfizer excess)
  • Risk Ratio (RR):
    ➔ 1.53 (i.e., 53% higher cardiovascular mortality risk)
  • Odds Ratio (Adjusted):
    ➔ 1.540 (95% CI: 1.431–1.657)

COVID-19 mortality

Pfizer recipients had nearly double the risk of COVID-19 death compared to Moderna recipients.

  • Pfizer Risk: 55.5 deaths per 100,000 people
  • Moderna Risk: 29.5 deaths per 100,000 people
  • Risk Difference:
    ➔ +26.0 deaths per 100,000 (Pfizer excess)
  • Risk Ratio (RR):
    ➔ 1.88 (i.e., 88% higher COVID-19 mortality risk)
  • Odds Ratio (Adjusted):
    ➔ 1.882 (95% CI: 1.596–2.220)

Non-COVID-19 mortality

Pfizer recipients faced a 35% higher risk of dying from non-COVID causes compared to Moderna recipients.

  • Pfizer Risk: 791.6 deaths per 100,000 people
  • Moderna Risk: 588.4 deaths per 100,000 people
  • Risk Difference:
    ➔ +203.3 deaths per 100,000 (Pfizer excess)
  • Risk Ratio (RR):
    ➔ 1.35 (i.e., 35% higher non-COVID mortality risk)
  • Odds Ratio (Adjusted):
    ➔ 1.356 (95% CI: 1.303–1.412)

Biological explanations

The findings of this study are surprising, given that Moderna’s mRNA-1273 vaccine contains approximately three times more mRNA (100 µg) than Pfizer’s BNT162b2 vaccine (30 µg). This suggests that the higher mortality observed among Pfizer recipients could potentially be related to higher levels of DNA contamination — an issue that has been consistently reported worldwide:

The paper hypothesizes differences between Pfizer and Moderna may be due to:

  • Different lipid nanoparticle compositions
  • Differences in manufacturing, biodistribution, or storage conditions

Final conclusion

Florida adults who received Pfizer’s BNT162b2 vaccine had higher 12-month risks of all-cause, cardiovascular, COVID-19, and non-COVID-19 mortality compared to Moderna’s mRNA-1273 vaccine recipients.

Unfortunately, without an unvaccinated group, the study cannot determine the absolute increase in mortality risk attributable to mRNA vaccination itself. However, based on the mountain of existing evidence, it is likely that an unvaccinated cohort would have experienced much lower mortality risks. It’s also important to remember that Moderna mRNA injections are still dangerous.

As the authors conclude:

These findings are suggestive of differential non-specific effects of the BNT162b2 and mRNA-1273 COVID-19 vaccines, and potential concerning adverse effects on all-cause and cardiovascular mortality. They underscore the need to evaluate vaccines using clinical endpoints that extend beyond their targeted diseases.

Nicolas Hulscher, MPH

Epidemiologist and Foundation Administrator, McCullough Foundation

www.mcculloughfnd.org

Please consider following both the McCullough Foundation and my personal accounton X (formerly Twitter) for further content.

Reprinted with permission from Focal Points.

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COVID-19

Canada’s health department warns COVID vaccine injury payouts to exceed $75 million budget

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Fr0m LifeSiteNews

By Clare Marie Merkowsky

A Department of Health memo warns that Canada’s Vaccine Injury Support Program will exceed its $75 million budget due to high demand, with $16 million already paid out.

COVID vaccine injury payments are expected to go over budget, according to a Canadian Department of Health memo.

According to information published April 28 by Blacklock’s Reporter, the Department of Health will exceed their projected payouts for COVID vaccine injuries, despite already spending $16 million on compensating those harmed by the once-mandated experimental shots.

“A total $75 million in funding has been earmarked for the first five years of the program and $9 million on an ongoing basis,” the December memo read. “However the overall cost of the program is dependent on the volume of claims and compensation awarded over time, and that the demand remains at very high levels.”

“The purpose of this funding is to ensure people in Canada who experience a serious and permanent injury as a result of receiving a Health Canada authorized vaccine administered in Canada on or after December 8, 2020 have access to a fair and timely financial support mechanism,” it continued.

Canada’s Vaccine Injury Support Program (VISP) was launched in December 2020 after the Canadian government gave vaccine makers a shield from liability regarding COVID-19 jab-related injuries.

While Parliament originally budgeted $75 million, thousands of Canadians have filed claims after received the so-called “safe and effective” COVID shots. Of the 3,060 claims received to date, only 219 had been approved so far, with payouts totaling over $16 million.

Since the start of the COVID crisis, official data shows that the virus has been listed as the cause of death for less than 20 kids in Canada under age 15. This is out of six million children in the age group.

The COVID jabs approved in Canada have also been associated with severe side effects such as blood clots, rashes, miscarriages, and even heart attacks in young, healthy men.

Additionally, a recent study done by researchers with Canada-based Correlation Research in the Public Interest showed that 17 countries have found a “definite causal link” between peaks in all-cause mortality and the fast rollouts of the COVID shots as well as boosters.

Interestingly, while the Department of Health has spent $16 million on injury payouts, the Liberal government spent $54 million COVID propaganda promoting the vaccine to young Canadians.

The Public Health Agency of Canada especially targeted young Canadians ages 18-24 because they “may play down the seriousness of the situation.”

The campaign took place despite the fact that the Liberal government knew about COVID vaccine injuries, according to a secret memo.

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