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Texas sues Pfizer for allegedly lying about COVID shot efficacy rate, trying to censor jab critics

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Ken Paxton, Texas Attorney General

From LifeSiteNews

By Ashley Sadler

‘The facts are clear. Pfizer did not tell the truth about their COVID-19 vaccines,’ Texas Attorney General Ken Paxton

Texas Republican Attorney General Ken Paxton on Thursday announced a lawsuit against Pfizer for allegedly misrepresenting the efficacy of their COVID-19 shots and attempting to squelch public criticism of the experimental drug. Pfizer responded, stating the company “has no higher priority than the safety and effectiveness of its treatments and vaccines” and believes Paxton’s “case has no merit.”

Paxton filed the 54-page complaint with the District Court of Lubbock County, Texas in a bid to “hold Pfizer responsible for its scheme of serial misrepresentations and deceptive trade practices” in violation of the Texas Deceptive Trade Practices Act.

“The facts are clear. Pfizer did not tell the truth about their COVID-19 vaccines,” the attorney general said in a November 30 press release announcing the lawsuit.

“The COVID-19 vaccines are the miracle that wasn’t,” the complaint states. “Pfizer intentionally misrepresented the efficacy of its COVID-19 vaccine and censored persons who threatened to disseminate the truth in order to facilitate fast adoption of the product and expand its commercial opportunity.”

According to the lawsuit, the advertised 95% efficacy of Pfizer’s COVID jab in people without prior infection led Americans to believe that the shot “would end the coronavirus pandemic” while in reality it did not. 

In fact, the lawsuit notes, “More Americans died in 2021, with Pfizer’s vaccine available, than in 2020, the first year of the pandemic.” Per the CDC, 384,536 people died with COVID-19 “listed as the underlying or contributing cause” in 2020, before the jab rollout, compared with 460,513 in 2021. 

“Pfizer’s product, buoyed by the company’s misrepresentations, enriched the company enormously,” the lawsuit states. Pfizer reportedly brought in $37.8 billion in revenue from its oft-mandated mRNA shots in 2021.

“But, while Pfizer’s misrepresentations piled up, its vaccine’s performance plummeted,” the Texas lawsuit states. 

The efficacy of all COVID jabs approved for use in the U.S., including Pfizer’s mRNA shot, fell significantly during 2021. Between February and October, the Pfizer jab’s reported efficacy was nearly cut in half, dropping from an estimated 86% to just 43% as calls for booster shots ramped up.

The lawsuit further alleges that Pfizer resorted to censorship attempts when its product failed to meet efficacy expectations.

“Pfizer labeled as ‘criminals’ those who spread facts about the vaccine. It accused them of spreading ‘misinformation,’” the lawsuit states. In November 2021, Pfizer CEO Alberto Bourla argued that people who steered others away from getting jabbed were “criminals.”

READ: Pfizer CEO: People spreading vax ‘misinformation’ are ‘criminals’ responsible for ‘millions’ of deaths

The lawsuit also alleges that Pfizer “coerced social media platforms to silence prominent truth-tellers.”

According to an installment of the “Twitter Files” by reporter Alex Berenson, Pfizer board member Dr. Scott Gottlieb, who formerly headed up the FDA, pushed Twitter to censor content expressing skepticism of the mRNA COVID shots.

Moreover, the lawsuit cited a report by journalist Lee Fang that found that the biopharmaceutical lobby group BIO “fully funded a special content moderation campaign designed by a contractor called Public Good Projects,” which worked with the social media platforms “to set content moderation rules around covid ‘misinformation.’”

Fang said BIO spent “$1,275,000 in funding for the effort, which included tools for the public to flag content on Twitter, Instagram, and Facebook for moderation.” While the campaign mostly flagged actual inaccuracies, it also included “requests to label or take down content critical of vaccine passports and government mandates to require vaccination.”

RELATED: WHO, EU announce partnership creating ‘global system’ of digital vaccine passports

On Thursday, Paxton said his office is “pursuing justice for the people of Texas, many of whom were coerced by tyrannical vaccine mandates to take a defective product sold by lies.”

Arguing that the Biden administration “weaponized the pandemic to force illegal public health decrees on the public and enrich pharmaceutical companies,” Paxton vowed to “use every tool I have to protect our citizens who were misled and harmed by Pfizer’s actions.”

In a statement to The Hill, Pfizer responded by saying it “is deeply committed to the well-being of the patients it serves and has no higher priority than the safety and effectiveness of its treatments and vaccines.”

“Since its initial authorization by FDA in December 2020, the Pfizer-BioNTech COVID-19 vaccine has been administered to more than 1.5 billion people, demonstrated a favorable safety profile in all age groups, and helped protect against severe COVID-19 outcomes, including hospitalization and death,” the drug company said. “The representations made by the company about its COVID-19 vaccine have been accurate and science-based.”

“The company believes that the state’s case has no merit and will respond to the petition in court in due course,” Pfizer added in its statement.

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COVID-19

FDA requires new warning on mRNA COVID shots due to heart damage in young men

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From LifeSiteNews

By Doug Mainwaring

Pfizer and Moderna’s mRNA COVID shots must now include warnings that they cause ‘extremely high risk’ of heart inflammation and irreversible damage in males up to age 24.

The Trump administration’s Food and Drug Administration (FDA) announced it will now require updated safety warnings on mRNA COVID-19 shots to include the “extremely high risk” of myocarditis/pericarditis and the likelihood of  long-term, irreversible heart damage for teen boys and young men up to age 24.

The required safety updates apply to Comirnaty, the mRNA COVID shot manufactured by Pfizer Inc., and Spikevax, the mRNA COVID shot manufactured ModernaTX, Inc.

According to a press release, the FDA now requires each of those manufacturers to update the warning about the risks of myocarditis and pericarditis to include information about:

  1. the estimated unadjusted incidence of myocarditis and/or pericarditis following administration of the 2023-2024 Formula of mRNA COVID-19 shots and
  2. the results of a study that collected information on cardiac magnetic resonance imaging (cardiac MRI) in people who developed myocarditis after receiving an mRNA COVID-19 injection.

The FDA has also required the manufacturers to describe the new safety information in the adverse reactions section of the prescribing information and in the information for recipients and caregivers.

Additionally, the fact sheets for healthcare providers and for recipients and caregivers for Moderna COVID-19 shot and Pfizer-BioNTech COVID-19 shot, which are authorized for emergency use in individuals 6 months through 11 years of age, have also been updated to include the new safety information in alignment with the Comirnaty and Spikevax prescribing information and information for recipients and caregivers.

In a video published on social media, Dr. Vinay Prasad, director of the Center for Biologics Evaluation & Research Chief Medical and Scientific Officer, explained the alarming reasons for the warning updates.

While heart problems arose in approximately 8 out of 1 million persons ages 6 months to 64 years following reception of the cited shots, that number more than triples to 27 per million for males ages 12 to 24.

Prasad noted that multiple studies have arrived at similar findings.

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COVID-19

Court compels RCMP and TD Bank to hand over records related to freezing of peaceful protestor’s bank accounts

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Justice Centre for Constitutional Freedoms

The Justice Centre for Constitutional Freedoms announces that a judge of the Ontario Court of Justice has ordered the RCMP and TD Bank to produce records relating to the freezing of Mr. Evan Blackman’s bank accounts during the 2022 Freedom Convoy protest.

Mr. Blackman was arrested in downtown Ottawa on February 18, 2022, during the federal government’s unprecedented use of the Emergencies Act. He was charged with mischief and obstruction, but he was acquitted of these charges at trial in October 2023. 

However, the Crown appealed Mr. Blackman’s acquittal in 2024, and a new trial is scheduled to begin on August 14, 2025. 

Mr. Blackman is seeking the records concerning the freezing of his bank accounts to support an application under the Charter at his upcoming retrial.

His lawyers plan to argue that the freezing of his bank accounts was a serious violation of his rights, and are asking the court to stay the case accordingly.

“The freezing of Mr. Blackman’s bank accounts was an extreme overreach on the part of the police and the federal government,” says constitutional lawyer Chris Fleury.

“These records will hopefully reveal exactly how and why Mr. Blackman’s accounts were frozen,” he says.

Mr. Blackman agreed, saying, “I’m delighted that we will finally get records that may reveal why my bank accounts were frozen.” 

This ruling marks a significant step in what is believed to be the first criminal case in Canada involving a proposed Charter application based on the freezing of personal bank accounts under the Emergencies Act. 

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