COVID-19
Kansas AG sues Pfizer for misrepresenting COVID shot as ‘safe and effective’

Kansas Attorney General Kris Kobach sues Pfizer for falsely claiming COVID shot is ‘safe and effective’
From LifeSiteNews
Kansas’s approach of attempting to penalize Pfizer for misrepresenting the shots’ risks, rather than the risks themselves, could help get around the PREP Act, and if successful would establish a model for other states to follow.
Kansas Republican Attorney General Kris Kobach announced on Monday that he is suing pharmaceutical giant Pfizer over “multiple misleading statements” about the health risks and ineffectiveness of its mRNA-based COVID-19 shot, in a case that if successful could mark a turning point in the ongoing battle against the controversial injections.
“Pfizer misled Kansans about the vaccines’ risks, including to pregnant women and for myocarditis,” the complaint states, according to a press release from the attorney general’s office. “Additionally, Pfizer claimed its vaccine protected against COVID variants, despite data showing otherwise. The pharmaceutical giant also suggested its vaccine prevented COVID transmission, but later admitted it had never studied whether its vaccine stopped transmission.”
“The complaint also alleges that Pfizer coordinated with social media officials to censor speech critical of COVID-19 vaccines and declined to participate in the federal government’s vaccine development program, Operation Warp Speed, to avoid government oversight,” Kobach’s office further says.
READ: The Telegraph admits COVID shots may have helped cause over 3 million excess deaths
Among its attempts to deceive the public, Pfizer maintained its own adverse event database, which included cases not reported to the federal Vaccine Adverse Event Reporting System (VAERS), but “did not publicly release adverse events data from its database.” It also “did not disclose that its trial included only healthy individuals and excluded unhealthy individuals” and therefore “did not possess a reasonable basis to represent that it was safe for individuals who had been diagnosed with COVID-19, who were immunocompromised, or who were pregnant or breastfeeding,” according to the lawsuit.
The complaint maintains that Pfizer’s misrepresentations, which helped the company earn $75 billion in two years, constitute violations of the Kansas Consumer Protection Act, “regardless of whether any individual consumer ultimately received Pfizer’s COVID-19 vaccine.”
In a statement to Fox Business, Pfizer responded that its claims “have been accurate and science-based. The Company believes that the state’s case has no merit and will respond to the suit in due course.”
READ: Pfizer reportedly withheld presence of cancer-linked DNA in COVID jabs from FDA, Health Canada
A significant body of evidence links significant risks to the COVID shots, which were developed and reviewed in a fraction of the time vaccines usually take under former President Donald Trump’s Operation Warp Speed initiative. Among it, VAERS reports 37,647 deaths, 216,757 hospitalizations, 21,741 heart attacks, and 28,445 myocarditis and pericarditis cases as of May 31, among other ailments. U.S. Centers for Disease Control & Prevention (CDC) researchers have recognized a “high verification rate of reports of myocarditis to VAERS after mRNA-based COVID-19 vaccination,” leading to the conclusion that “under-reporting is more likely” than over-reporting.
An analysis of 99 million people across eight countries published February in the journal Vaccine – the largest analysis to date – “observed significantly higher risks of myocarditis following the first, second and third doses” of mRNA-based COVID jabs, as well as signs of increased risk of “pericarditis, Guillain-Barré syndrome, and cerebral venous sinus thrombosis,” and other “potential safety signals that require further investigation.” In April, the CDC was forced to release by court order 780,000 previously undisclosed reports of serious adverse reactions, and a study out of Japan found “statistically significant increases” in cancer deaths after third doses of mRNA-based COVID-19 shots and offered several theories for a causal link.
READ: Canadian father files $35 million lawsuit against Pfizer over son’s jab-related death
In Florida, a grand jury impaneled by Republican Gov. Ron DeSantis is currently investigating the manufacture and rollout of the COVID shots. In February, it released its first interim report on the underlying justification for Operation Warp Speed, which determined that lockdowns did more harm than good, that masks were ineffective at stopping COVID transmission, that COVID was “statistically almost harmless” to children and most adults, and that it is “highly likely” that COVID hospitalization numbers were inflated. The grand jury’s report on the jabs themselves is highly anticipated.
One long-standing impediment to holding Big Pharma accountable for the above issues has been the federal Public Readiness & Emergency Preparedness (PREP) Act of 2005, which, according to the Congressional Research Service (CRS), empowers the federal government to “limit legal liability for losses relating to the administration of medical countermeasures such as diagnostics, treatments, and vaccines.” Near the beginning of the COVID outbreak, the U.S. Department of Health & Human Services (HHS) invoked the act in declaring the virus a “public health emergency.”
READ: 33-year-old father dies of immune disorder linked to Pfizer COVID vaccine, doctors say
Under this “sweeping” immunity, CRS explains, the federal government, state governments, “manufacturers and distributors of covered countermeasures,” and licensed or otherwise-authorized health professionals distributing those countermeasures are shielded from “all claims of loss” stemming from those countermeasures, with the exception of “death or serious physical injury” brought about through “willful misconduct,” a standard that, among other hurdles, requires the offender to have acted “intentionally to achieve a wrongful purpose.”
Kansas’s approach of attempting to penalize Pfizer for misrepresenting the shots’ risks, rather than the risks themselves, could help get around the PREP Act, and if successful would establish a model for other states to follow.
2025 Federal Election
Conservatives promise to ban firing of Canadian federal workers based on COVID jab status

From LifeSiteNews
The Conservative platform also vows that the party will oppose mandatory digital ID systems and a central bank digital currency if elected.
Pierre Poilievre’s Conservative Party’s 2025 election platform includes a promise to “ban” the firing of any federal worker based “solely” on whether or not they chose to get the COVID shots.
On page 23 of the “Canada First – For A Change” plan, which was released on Tuesday, the promise to protect un-jabbed federal workers is mentioned under “Protect Personal Autonomy, Privacy, and Data Security.”
It promises that a Conservative government will “Ban the dismissal of federal workers based solely on COVID vaccine status.”
The Conservative Party also promises to “Oppose any move toward mandatory digital ID systems” as well as “Prohibit the Bank of Canada from developing or implementing a central bank digital currency.”
In October 2021, the Liberal government of former Prime Minister Justin Trudeau announced unprecedented COVID-19 jab mandates for all federal workers and those in the transportation sector. The government also announced that the unjabbed would no longer be able to travel by air, boat, or train, both domestically and internationally.
This policy resulted in thousands losing their jobs or being placed on leave for non-compliance. It also trapped “unvaccinated” Canadians in the country.
COVID jab mandates, which also came from provincial governments with the support of the federal government, split Canadian society. The shots have been linked to a multitude of negative and often severe side effects, such as death, including in children.
Many recent rulings have gone in favor of those who chose not to get the shots and were fired as a result, such as an arbitrator ruling that one of the nation’s leading hospitals in Ontario must compensate 82 healthcare workers terminated after refusing to get the jabs.
Beyond health concerns, many Canadians, especially Catholics, opposed the injections on moral grounds because of their link to fetal cell lines derived from the tissue of aborted babies.
COVID-19
RFK Jr. Launches Long-Awaited Offensive Against COVID-19 mRNA Shots

Nicolas Hulscher, MPH
As millions of Americans anxiously await action from the new HHS leadership against the COVID-19 mRNA injections—injected into over 9 million children this year—Robert F. Kennedy Jr. has finally gone publicly on the offensive:
Let’s go over each key point made by RFK Jr.:
The recommendation for children was always dubious. It was dubious because kids had almost no risk for COVID-19. Certain kids that had very profound morbidities may have a slight risk. Most kids don’t.
In the largest review to date on myocarditis following SARS-CoV-2 infection vs. COVID-19 vaccination, Mead et al found that vaccine-induced myocarditis is not only significantly more common but also more severe—particularly in children and young males. Our findings make clear that the risks of the shots overwhelmingly outweigh any theoretical benefit:
The OpenSAFELY study included more than 1 million adolescents and children and found that myocarditis was documented ONLY in COVID-19 vaccinated groups and NOT after COVID-19 infection. There were NO COVID-19-related deaths in any group. A&E attendance and unplanned hospitalization were higher after first vaccination compared to unvaccinated groups:
So why are we giving this to tens of millions of kids when the vaccine itself does have profound risk? We’ve seen huge associations of myocarditis and pericarditis with strokes, with other injuries, with neurological injuries.
The two largest COVID-19 vaccine safety studies ever conducted, involving 99 million (Faksova et al) and 85 million people (Raheleh et al), confirm RFK Jr.’s concerns, documenting significantly increased risks of serious adverse events following vaccination, including:
- Myocarditis (+510% after second dose)
- Acute Disseminated Encephalomyelitis (+278% after first dose)
- Cerebral Venous Sinus Thrombosis (+223% after first dose)
- Guillain-Barré Syndrome (+149% after first dose)
- Heart Attack (+286% after second dose)
- Stroke (+240% after first dose)
- Coronary Artery Disease (+244% after second dose)
- Cardiac Arrhythmia (+199% after first dose)
And this was clear even in the clinical data that came out of Pfizer. There were actually more deaths. There were about 23% more deaths in the vaccine group than the placebo group. We need to ask questions and we need to consult with parents.
Actually, according to the Pfizer’s clinical trial data, there were 43% more deaths in the vaccine group compared to the placebo group when post-unblinding deaths are included:
We need to give people informed consent, and we shouldn’t be making recommendations that are not good for the population.
Public acknowledgment of the grave harms of COVID-19 vaccines signals that real action is right around the corner. However, we must hope that action is taken for ALL age groups, as no one is spared from their life-reducing effects:
Alessandria et al (n=290,727, age > 10 years): People vaccinated with 2 doses lost 37% of life expectancy compared to the unvaccinated population during follow-up.
Epidemiologist and Foundation Administrator, McCullough Foundation
Please consider following both the McCullough Foundation and my personal account on X (formerly Twitter) for further content.
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