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Report Shows Politics Trumped Science on U.S. Vaccine Mandates

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From the Frontier Centre for Public Policy

By Lee Harding

If you thought responsible science drove the bus on the pandemic response, think again. A December 2024 report by the U.S. House of Representatives Select Subcommittee, Coronavirus Pandemic shows that political agendas made regulatory bodies rush vaccine approvals, mandates, and boosters, causing public distrust.

ā€œAfter Action Review of the COVID-19 Pandemic: The Lessons Learned and a Path Forwardā€ praised the Trump administration’s efforts to speed up vaccine development. By contrast, the report said presidential candidate Joe Biden and vice-presidential candidate Kamala Harris undermined public confidence.

ā€œ[W]hy do we think the public is gonna line up to be willing to take the injection?ā€ Joe Biden asked on September 5, 2020. This quote appeared in aĀ PoliticoĀ article titled ā€œHarris says she wouldn’t trust Trump on any vaccine released before [the] election.ā€

The House report noted, ā€œThese irresponsible statements eventually proved to be outright hypocrisy less than a year later when the Biden-Harris Administration began to boldly decry all individuals who decided to forgo COVID-19 vaccinations for personal, religious, or medical reasons.ā€

Millions of doses of COVID-19 vaccines were administered beginning in December 2020 under anĀ Emergency Use Authorization. This mechanism allows unapproved medical products to be used in emergency situations under certain criteria, including that there are no alternatives. The only previous EUA was for the 2004 anthrax vaccine, which was only administered to a narrow group of people.

By the time vaccines rolled out, SARS-CoV-2 had already infected 91 million Americans. The original SARS virus some 15 years prior showed that people who recovered had lasting immunity. Later, a January 2021 study of 200 participants by the La Jolla Institute of Immunology found 95 per cent of people who had contracted SARS-CoV-2 (the virus behind COVID-19) had lasting immune responses. A February 16, 2023 article by Caroline Stein inĀ The LancetĀ (updated March 11, 2023) showed that contracting COVID-19 provided an immune response that was as good or better than two COVID-19 shots.

Correspondence suggests that part of the motivation for full (and not just emergency) vaccine approval was to facilitate vaccine mandates. A July 21, 2021, email from Dr. Marion Gruber, then director of vaccine reviews for the Food and Drug Administration (FDA), recalled that Dr. Janet Woodcock had stated that ā€œabsent a license, states cannot require mandatory vaccination.ā€ Woodcock was the FDA’s Principal Deputy Commissioner at the time.

Sure enough, the FDA granted full vaccine approval on August 23, 2021, more than four months sooner than a normal priority process would take. Yet, five days prior, Biden made an announcement that put pressure on regulators.

On August 18, 2021, Biden announced that all Americans would have booster shots available starting the week of September 20, pending final evaluation from the FDA and the U.S. Centers for Disease Control and Prevention (CDC).

Some decision-makers objected. Dr. Marion Gruber and fellow FDA deputy director of vaccine research Dr. Philip Krause had concerns regarding the hasty timelines for approving Pfizer’s primary shots and boosters. On August 31, 2021, they announced their retirements.

According to a contemporaryĀ New York TimesĀ article, Krause and Gruber were upset about Biden’s booster announcement. The article said that ā€œneither believed there was enough data to justify offering booster shots yet,ā€ and that they ā€œviewed the announcement, amplified by President Biden, as pressure on the F.D.A. to quickly authorize them.ā€

InĀ The LancetĀ on September 13, 2021, Gruber, Krause, and 16 other scientists warned that mass boosting risked triggering myocarditis (heart inflammation) for little benefit.

ā€œ[W]idespread boosting should be undertaken only if there is clear evidence that it is appropriate,ā€ the authors wrote. ā€œCurrent evidence does not, therefore, appear to show a need for boosting in the general population, in which efficacy against severe disease remains high.ā€

Regardless, approval for the boosters arrived on schedule on September 24, 2021. CDC Director Dr. Rochelle Walensky granted this approval, but for a wider population than recommended by her advisory panel. This was only the second time in CDC history that a director had defied panel advice.

ā€œ[T]his process may have been tainted with political pressure,ā€ the House report found.

Amidst all this, the vaccines were fully licensed. The FDA licensed the Comirnaty (Pfizer-BioNTech) vaccine on August 23, 2021. The very next day, Defense Secretary Lloyd Austin issued a memo announcing a vaccine mandate for the military. Four other federal mandates followed.

ā€œ[T]he public’s perception [is] that these vaccines were approved in a hurry to satisfy a political agenda,ā€ the House report found.

The House report condemned the dubious process and basis for these mandates. It said the mandates ā€œignored natural immunity, … risk of adverse events from the vaccine, as well as the fact that the vaccines don’t prevent the spread of COVID-19.ā€

The mandates robbed people of their livelihoods, ā€œhollowed out our healthcare and education workforces, reduced our military readiness and recruitment, caused vaccine hesitancy, reduced trust in public health, trampled individual freedoms, deepened political divisions, and interfered in the patient-physician relationship,ā€ the report continued.

The same could be said of Canadian vaccine mandates, as shown by the National Citizen’s Inquiry hearings on COVID-19. Unfortunately, an official federal investigation and a resulting acknowledgement do not seem forthcoming. Politicized mandates led to profits for vaccine manufacturers but left ā€œscienceā€ with a sullied reputation.

Lee HardingĀ is a Research Fellow for the Frontier Centre for Public Policy.

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Sen. Rand Paul: ā€˜I am officially re-referring Dr. Fauci to the DOJ’

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Fr0m LifeSiteNews

By Doug Mainwaring

ā€˜Perjury is a crime,’ Sen. Rand Paul declared on X. ā€˜And Fauci must be held accountable.’

Sen. Rand Paul announced Monday that he is again pressuring the U.S. Department of Justice (DOJ) to launch a criminal probe of Dr. Anthony Fauci afterĀ The New York TimesĀ revealed his 11th-hour pardon by the Biden administration is likely invalid.

ā€œToday, I will reissue my criminal referral of Anthony Fauci to Trump DOJ!ā€Ā declaredĀ Paul, laterĀ adding, ā€œPerjury is a crime. And Fauci must be held accountable.ā€

By late in the afternoon on Monday, the Kentucky senator had composed a letter to Attorney General Pam Bondi citing the times he believed Fauci had lied under oath during congressional hearings and urging the DOJ to finally investigate Fauci.

ā€œIn July 2023, I referred Dr. Anthony Fauci to the Department of Justice for lying under oath to Congress. His own emails directly contradicted his sworn testimony,ā€ PaulĀ wroteĀ X.

ā€œNYT reports Fauci was quietly pardoned by an autopen, operated by Biden’s staff. If the President didn’t authorize this pardon personally, then the Department has a duty to investigate and prosecute as it would any ordinary citizen,ā€ Paul said.

ā€œFauci has been sainted by the extremist Left, but it doesn’t erase his lying before Congress,ā€ Paul said. ā€œI am officially re-referring Dr. Fauci to the DOJ.ā€

Sen. Paul concluded his letter to Bondi by explaining that his autopen pardon is now seen to be illegitimate:

On January 19, 2025, Dr. Fauci was issued a full and unconditional pardon for any offenses that he may have committed or taken part in since 2014. Dr. Fauci was included among a group of individuals granted unprecedented preemptive pardons on President Joe Biden’s final day in office. However, new information has revealed that these pardons were executed via autopen, with no documented confirmation that the President personally reviewed or approved each individual grant of clemency.

According to reports, White House staff authorized the use of the autopen to issue the clemency documents. This raises serious constitutional and legal concerns about the legitimacy of Dr. Fauci’s Pardon.

President Donald TrumpĀ toldĀ reporters on Monday that the constant reliance on the autopen by the Biden administration is ā€œone of the biggest scandals that we’ve had in 50 to 100 years.ā€

ā€œI guarantee (Biden) knew nothing about what he was signing,ā€ Trump asserted.

Fauci’s mendacious relationship with CongressĀ 

The senator from the Bluegrass State and Dr. Fauci have long had aĀ combativeĀ relationship.

In 2021, Sen. Paul alleged that Fauci, who then served as director of the National Institutes of Allergy and Infectious Disease (NIAID) and as medical adviser to former President Joe Biden, ā€œlied to Congressā€ when heĀ claimedĀ that the National Institutes of Health (NIH), of which the NIAID is a part, was not funding and had never funded ā€œgain-of-functionā€ research in Wuhan, China.

Then in 2023, Paul again filed a criminal referral to the DOJ against the White House COVID czar for lying to Congress about his role in subsidizing controversial gain-of-function (GOF) research that was suspected of contributing to the COVID outbreak.

ā€œWe have him dead to rights, the problem is this: we have Merrick Garland who I think is a pure rank partisan,ā€ Paul said at the time. ā€œI don’t think he’ll ever be prosecuted. We also have a Democrat Party that is happy to have paid him more than the president, more than any president makes and he actually got a million dollars from a private foundation while he was still a public servant. Everything about this is rotten to the core and if we don’t bring him to justice we’ll never get the control we need on this type of research to try and prevent it from happening again.ā€

Paul has said multiple times that Dr. Fauci should ā€œgo to prisonā€ for lying to Congress.

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Conservatives demand probe into Liberal vaccine injury program’s $50m mismanagement

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From LifeSiteNews

By Clare Marie Merkowsky

The Liberals’ Vaccine Injury Support Program is accused of mismanaging a $50-million contract with Oxaro Inc. and failing to resolve claims for thousands of vaccine-injured Canadians.

Conservatives are calling for an official investigation into the Liberal-run vaccine injury program, which has cost Canadians millions but has little to show for it.

On July 14th, four Conservative Members of Parliament (MPs)Ā signedĀ a letter demanding answers after an explosiveĀ Global News report found the Liberals’ Vaccine Injury Support Program (VISP) misallocated taxpayer funds and disregarded many vaccine-injured Canadians.

ā€œThe federal government awarded a $50 million taxpayer-funded contract to Oxaro Inc. (formerly Raymond Chabot Grant Thornton Consulting Inc.). The purpose of this contract was to administer the VISP,ā€ the letter wrote.

ā€œHowever, there was no clear indication that Oxaro had credible experience in healthcare or in the administration of health-related claims raising valid questions about how and why this firm was selected,ā€ it continued.

Canada’s VISPĀ was launchedĀ in December 2020 after the Canadian government gave vaccine makers a shield from liability regarding COVID-19 jab-related injuries.

However, mismanagement within the program has led to many injured Canadians still waiting to receive compensation, while government contractors grow richer.

ā€œDespite the $50 million contract, over 1,700 of the 3,100 claims remain unresolved,ā€ the Conservatives continued. ā€œFamilies dealing with life-altering injuries have been left waiting years for answers and support they were promised.ā€

Furthermore, the claims do not represent the total number of Canadians injured by the allegedly ā€œsafe and effectiveā€ COVID shots, as inside memosĀ have revealedĀ that the Public Health Agency of Canada (PHAC) officials neglected to report all adverse effects from COVID shots and even went as far as telling staff not to report all events.

The PHAC’s downplaying of vaccine injuries is of little surprise to Canadians, as aĀ 2023Ā secret memo revealed that the federal government purposefully hid adverse effect so as not to alarm Canadians.

The letter further revealed that former VISP employees have revealed that the program lacked professionalism, describing what Conservatives described as ā€œa fraternity house rather than a professional organization responsible for administering health-related claims.ā€

ā€œReports of constant workplace drinking, ping pong, and Netflix are a slap in the face to taxpayers and the thousands of Canadians waiting for support for life altering injuries,ā€ the letter continued.

Regardless of this, the Liberal government, under Prime Minister Mark Carney, is considering renewing its contract with Oxaro Inc.

Indeed, this would hardly be the first time that Liberals throw taxpayer dollars at a COVID program that is later exposed as ineffective and mismanaged.

Canada’s infamous ArriveCan app, which was mandated for all travelers in and out of Canada in 2020, has cost Canadians $54 million, despite the Public Health Agency of CanadaĀ admittingĀ that they have no evidence that the program saved lives.

Details regarding the app and the government contracts surrounding it have been hidden from Canadians, as Liberals wereĀ exposed in 2023 for hiding a RCMP investigation into the app from auditors.

An investigation of the ArriveCan appĀ beganĀ in 2022 after the House of Commons voted 173-149 for a full audit of theĀ controversial app.

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