Genomics Expert Who Discovered DNA Contamination in mRNA Shots Accuses Regulators of Lying About Cancer Risks

Moderna COVID Vaccine

The scientist who first blew the whistle on the DNA contamination in the COVID mRNA injections last year, said Monday that regulators and fact checkers have been “continually wrong” about his alarming discovery, downplaying its significance and telling flat out lies about the potential dangers.

Last April, microbiologist Kevin McKernan, published a paper establishing that simian virus 40 (SV40), a virus found in monkeys and humans, is present in Pfizer and Moderna’s mRNA COVID-19 injections. The discovery was highly significant because SV40 has been linked to cancer in humans, and since the rollout of the mRNA products, the western world has seen a dramatic increase in cancers, especially in previously healthy working aged people.

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Commentary: Pediatrician Is Fighting Back as Her Medical License Is Being Investigated for COVID-19 ‘Misinformation’

Renata Moon

Once she saw the data, pediatrician Dr. Renata Moon knew she had to speak out. Over her more than 20 years of practicing medicine, including more than 17 years of treating high-risk patients, Dr. Moon had never been anti-vaccine—until she saw what was happening with the COVID-19 vaccines.

In Dr. Moon’s words: “As the data rolled out on the vaccine and COVID-19, it became clear that children had basically a zero risk of death from infection by COVID [whereas] they have potential serious risk from taking the COVID-19 shots.”

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Texas AG Ken Paxton Sues Pfizer for Misrepresenting Efficacy of the COVID-19 Jabs and Conspiring to Censor Public Discourse

AG Ken Paxton

Texas Attorney General Ken Paxton announced Thursday that he is suing Pfizer for “unlawfully misrepresenting” Covid-19 vaccine efficacy and conspiring to censor public discourse.

“Pfizer engaged in false, deceptive, and misleading acts and practices by making unsupported claims regarding the company’s COVID-19 vaccine in violation of the Texas Deceptive Trade Practices Act,” Paxton said in a press release.

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Dr. Malone: Pfizer and Moderna Committed Fraud by Not Disclosing to Regulators COVID Jabs Contaminated with DNA Fragments

Pfizer and Moderna’s lack of transparency regarding DNA contamination in its COVID-19 shots “meets the criteria for evidence of fraud,” according to the doctor who invented the mRNA vaccine technology upon which the products are based.

“They [Pfizer and Moderna] absolutely did know about the existence of SV40 sequences,” vaccinologist Dr. Robert Malone told Republican lawmakers during a livestream House hearing Monday. Rep. Marjorie Taylor Greene (R-Ga.) led the event to examine injuries and deaths caused by COVID-19 vaccinations.

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FDA Blasted for ‘Misleading’ mRNA COVID Vaccine Labels as ‘Sudden Death’ Research Mounts

Researchers around the world continue documenting potentially severe side effects from COVID-19 mRNA vaccines in certain demographics, but the Food and Drug Administration refuses to label them or even tell recipients the shots can’t stop transmission of an increasingly immune-evasive virus.

Autopsies and reviews of medical records revealed a much higher incidence of Pfizer and Moderna vaccine-associated heart deaths than officially categorized in South Korean, Japanese and Qatari government registries, particularly in younger people at lower risk from COVID. That echoes a German autopsy study of healthy people who died within 20 days of jabs.

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Pfizer COVID Vaccine Safety Report Identified Nearly 1.6 Million Adverse Events Early On

By June of  2022, Pfizer had identified over 10,000 categories of nearly 1.6 million adverse events, a recently-released safety update report shows. Pfizer’s pharmacovigilance documents were requested and released by the European Medicines Agency, the EU’s drug regulator, Conservative Review’s Daniel Horowitz reported on Wednesday.

The 396-page confidential Pfizer report, dated August 18, 2022, reveals that Pfizer was well aware its product was causing an unacceptable level of serious and debilitating injuries early on.

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DOD ‘Bait and Switch’ with Emergency and Licensed COVID Vaccines Killed Student, Lawsuit Alleges

The Pentagon conducted “human experimentation without consent” by falsely advertising a COVID-19 vaccine under emergency use authorization as fully licensed, a “bait and switch” that killed a college student, according to a new lawsuit against Defense Secretary Lloyd Austin by the student’s estate.

George Watts was waiting for FDA approval of Pfizer’s Comirnaty to fulfill the COVID vaccine mandate at New York’s Corning Community College, which provided a 35-day grace period for compliance following Comirnaty’s Aug. 23, 2021, approval, the filing states.

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Pfizer Recalls Millions of Pills over Risk of Child Poisoning

Pfizer recalled more than four million packages of Nurtec ODT Thursday due to the risk of child poisoning, according to the United States Consumer Product Safety Commission (CPSC).

Pfizer is recalling the migraine medicine because it is currently in a blister packet, which is not deemed “child resistant” and therefore poses a potential risk to children. For a package to be child resistant, it must be significantly challenging for a child under five to open it, according to CPSC.

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Sen. Marco Rubio Cites Project Veritas Undercover Video in Letter to Pfizer CEO on Alleged Gain-of-Function Research

Florida U.S. Senator Marco Rubio (R) cited the most recent undercover investigation released by Project Veritas (PV) in a letter to Albert Bourla, CEO of Pfizer, and noted that, according to the PV video, Pfizer may be conducting gain-of-function research to mutate the COVID virus to create additional variants and vaccines to combat them for profit. Rubio’s office noted that, in the PV exposé, Pfizer executive Jordon Trishton Walker claimed the drug company is considering the possibility of mutating the COVID virus itself via “directed evolution” in order to keep profiting off a continued stream of vaccines – which he later said would be a “cash cow” for the company.

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Pfizer Executive Heard Claiming Company Considering Mutating COVID Virus Itself to Continue Profiting Off Vaccines, Later Seen Assaulting Project Veritas Founder James O’Keefe

A top-level Pfizer executive revealed to an undercover Project Veritas (PV) journalist that the pharmaceutical giant is considering the possibility of mutating the COVID virus itself via “directed evolution” in order to keep profiting off a continued stream of vaccines. Following the release of the first video, which was published Wednesday, Jordon Trishton Walker, Pfizer director of Research and Development, Strategic Operations – mRNA Scientific Planner, is seen in a second video assaulting PV founder James O’Keefe and his staff in a restaurant, and destroying the iPad showing the undercover video recordings.

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Wall Street Journal Rips Vaccine Makers: ‘Designed Studies to Get the Results They Wanted’

Wall Street Journal (WSJ) editorial board member Allysia Finley took to task both the federal government and the pharmaceutical giants profiting from the sale of their COVID mRNA booster shots for a “deceptive advertising” push for Americans to continue taking boosters without proof of their safety or effectiveness. The U.S. Department of Health and Human Services (HHS) and its health and regulatory agencies are engaged in a “deceptive advertising” campaign, wrote Finley Sunday, suggesting the pressure tactics “shouldn’t come as a surprise,” since the federal government “took the unprecedented step of ordering vaccine makers to produce them and recommending them without data supporting their safety or efficacy.”

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Pfizer, Fauci Staffers Sign Off on Research Finding mRNA COVID Vaccines Produce Worse Antibodies

Less than a month after the CDC marked the two-year anniversary of the first administered COVID-19 vaccine by telling Americans to get a bivalent booster, two peer-reviewed German studies have found that mRNA vaccines — the vast majority of the U.S. market — induce worse antibodies compared to traditional adenovirus vaccines. The first paper, published in Science Immunology Dec. 22, focused on mRNA boosters, while the second, published in Frontiers in Immunology Jan. 12, found the same association with the two-dose primary series.

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Pfizer and Moderna Conducting Studies to Assess Long-Term Impacts of Myocarditis

Nearly two years after their mRNA “vaccines” were released to the public, both Pfizer and Moderna are finally conducting clinical trials to track long-term adverse health effects following a diagnosis of vaccine-associated myocarditis and pericarditis in teens and young adults under the age of 21. Myocarditis  can cause permanent damage to heart muscle and even death.

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Biden FDA Approves COVID Booster Shot for Children 5-11 Years Old Without Testing

Pfizer Inc. and BioNTech announced Wednesday the Biden Food and Drug Administration (FDA) granted Emergency Use Authorization (EUA) for their “bivalent” mRNA COVID-19 booster shot for children aged 5-11 years without having completed clinical trials.

“As families across the country take part in fall festivities and plan for the upcoming holiday season, we aim to provide school-aged children with additional protection against the Omicron BA.4/BA.5 subvariants, which continue to account for more than 80% of cases in the U.S.,” said Pfizer CEO Albert Bourla. “Anticipating this need, we manufactured millions of booster doses, which will be made available, pending CDC recommendation, to help families stay up to date with COVID-19 vaccinations.”

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Pfizer Executive Admits COVID Vaccine Was Never Tested for Blocking Transmission of Virus

A top Pfizer international executive admitted to a European Parliament committee Tuesday that the pharmaceutical giant did not test its COVID mRNA shot for whether it could prevent transmission of the virus before it was placed on the market and then mandated in many parts of society throughout the world.

Rob Roos, a member of the European Parliament from the Netherlands, tweeted a video of his exchange with Janine Small, president of international developed markets at Pfizer.

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Woke Pfizer Policy Prohibits Whites and Asians from Applying for Fellowship

Drug giant Pfizer says its top-level “Breakthrough Fellowship Program” that prohibits whites and Asians from applying is a “Bold Move” that promotes “a more inclusive workplace,” and will have Pfizer led by “a new generation” of minority fellows by 2025.

“One of Pfizer’s Bold Moves is to create a workplace for all, and we are committed to increasing diversity by fostering a more inclusive workplace,” says Pfizer, one of the Big Pharma companies at the center of the controversial COVID-19 vaccines.

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Moderna Suing Pfizer for COVID-19 Vaccine Patent Infringement

Moderna is filing patent infringement lawsuits against Pfizer and BioNTech in U.S. district court and German regional court Friday in connection with the two companies’ COVID-19 vaccine, Moderna announced.

Moderna alleges Pfizer and BioNTech’s Comirnaty vaccine breaches its mRNA technology patents submitted between 2010 and 2016. It claims they developed their vaccine by copying the technology Moderna used to make its mRNA COVID-19 vaccine, Spikevax.

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Report: 44 Percent of Pregnant Women in Pfizer Vaccine Trial Lost Their Babies

More than 40 percent of pregnant women who participated in Pfizer’s mRNA COVID vaccine trial suffered miscarriages, according internal Pfizer documents, recently released under court order. Despite this, Pfizer, and the Biden administration insisted that the vaccines were safe for pregnant women. Out of 50 pregnant women, 22 of them lost their babies, according to an analysis of the documents.

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New Government Spending Will Benefit Top Biden Adviser’s Consulting Clients

White House Senior adviser Anita Dunn has consulted for companies and trade groups that have benefited or stand to benefit from federal funding and is being forced to recuse herself from matters involving them, according to a financial disclosure.

Dunn has consulted through the public affairs firm SKDK during the past two years for the likes of Pfizer, AT&T, Micron and the American Clean Power Association, according to a filing reported on by CNBC Friday. Dunn, who founded the SKDK in 2004, is recused from working on issues related to past clients, a spokesman for the White House told the Daily Caller News Foundation.

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Ivy League Study: Boosters, COVID-19 ‘Rebounds’ Fuel Skepticism of Federal Narratives

As the nation’s most powerful and twice-boosted infectious disease doctor battles a COVID-19 “rebound” two weeks after testing positive, new research from the public health schools at Harvard and Yale suggests the boosted fared worse against the first Omicron subvariant than the non-boosted.

The FDA is so alarmed by the “waning effectiveness” of boosters, whose formulation is still based on the ancestral Wuhan strain, that it asked manufacturers Thursday to add a “spike protein component” from the fourth and fifth Omicron subvariants to this fall’s boosters.

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Peer-Reviewed Paper Shows Significant Fertility Risks for Men Who Get the Pfizer COVID Vaccine

A peer-reviewed paper released on Friday shows large decreases in sperm counts among men after the second dose of Pfizer’s mRNA COVID vaccine, with the decline continuing for over five months in many cases.

The study, published in the medical journal Andrology, confirms that the mRNA shots have significant fertility risks for men, independent journalist Alex Berenson reported on his Unreported Truths Substack.

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Whisteblower’s Lawyer: Pfizer Got Away with Vaccine Fraud Because Government Was Co-Conspirator

Pfizer has asked a U.S. court to throw out a whistleblower’s lawsuit on the basis that the company can’t be guilty of fraud, abuse, and protocol violations in its COVID Vaccine clinical trials because its contract with the U.S. government allowed them to skirt regulations and federal laws that typically apply to government contracts.

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Doctor Crashes FDA Meeting and Shares the Whistleblower Story They Ignored

A doctor “crashed” a Food and Drug Administration’s meeting with outside vaccine experts earlier this week, to share a whistleblower’s story about the data integrity issues that plagued one of Pfizer’s clinical trials.

In September of 2020, a researcher from an organization testing Pfizer’s vaccine at several sites in Texas, emailed a complaint to the FDA, informing the agency of the company’s dangerously shoddy research practices. The FDA took no action on her email, and Pfizer continues to use the company.

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Newly Released Docs: Pfizer Had to Hire 1,800 Additional Employees in Early 2021 to Process ‘Large Increase’ in Vaccine Adverse Events

Pfizer hired 1,800 additional full-time employees in the first half of 2021 to deal with “the large increase” of adverse reactions to its COVID vaccine, newly released secret documents reveal. The Pfizer-BioNTech COVID-19 Vaccine was made available under the Emergency Use Authorization (EUA) on Dec. 11, 2020. By February of 2021, the company was seeing so many safety signals, including in pregnant and breastfeeding mothers, it had to immediately hire 600 employees to process the data.

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Pfizer CEO Calls for Another Booster Shot for All Americans

On Sunday, the chief executive officer of Pfizer said that Americans should be prepared to receive a second booster shot of the Coronavirus vaccine, which would mark the fourth overall shot that has been forced on the American public.

As reported by Politico, Albert Bourla made his remarks in an interview with CBS’ Margaret Brennan, where he said that his company was preparing to submit “a significant package of data about the need for a fourth dose” to the Food and Drug Administration (FDA).

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Trans Activists Funded by Big Pharma Push Biased Research Promoting Medical Transitions for Children

Researchers are churning out biased studies promoting medical gender transitions for children, often supported by pharmaceutical companies and activist organizations, and the media frequently promotes the conclusions uncritically.

A March 2021 National Institute for Health and Care Excellence comprehensive review of nine studies failed to find evidence that hormonal therapy and puberty blockers were helpful. The review pointed out common flaws in transgender treatment research, such as confounding variables and bias resulting from observational studies that lack control groups.

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