Arkansas Looks to Hold Pharma Execs Criminally Liable for Vaccine Injuries

Arkansas lawmakers are weighing legislation that could pierce the pharmaceutical industry’s federal liability shield for vaccine injuries by holding corporate executives criminally liable for “vaccine harms” if they concealed evidence of risks associated with a vaccine that subsequently seriously injured or killed the recipient.

Under Senate Bill 6, introduced by Republican State Sen. Bryan King, an executive officer of a pharmaceutical company that “knowingly hides, conceals, omits, or otherwise withholds evidence, documentation, or information that the vaccine has dangerous effects,” would be found guilty of a felony and face a prison sentence of one year to life.

The bill is pending before the Arkansas Senate. King also introduced Senate Bill 5, to hold Pharma executives criminally liable for “prescription drug harm.”

Previous versions of both bills unanimously passed last year in the Arkansas Senate but died in the Arkansas House.

Ray Flores, senior outside counsel for Children’s Health Defense (CHD), welcomed the proposed legislation. He told The Defender:

“Regarding vaccines and other health-related issues, the public is increasingly frustrated with the impervious protection current law and corporate structure afford. The time is ripe to single out those ultimate decision-makers who benefit the most.

“This is an attempt, done properly through legislation, to address that powerlessness currently radiating throughout society.”

California-based healthcare attorney Rick Jaffe called the proposed legislation “an excellent jumping-off point for the serious discussion the country needs to have about vaccines.”

King’s office did not respond to The Defender’s request for comment by press time.

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URGENT: Yale researchers have found Covid spike protein in the blood of people never infected with Covid – years after they got mRNA jabs

Yale University scientists have found Covid spike protein in the blood of people who received Covid mRNA shots – up to two years after they received the jabs.

The people were never infected with Covid, antibody tests show, and our immune systems rapidly destroy newly produced spike proteins. The finding suggests some people who took the shots may be making the proteins on their own.

A possible reason is that genetic material delivered in the shots has integrated with human genes and is continuing to activate protein-making structures in our cells. If found to be correct, this explanation has serious implications for mRNA vaccine safety and the more than 1 billion people who received mRNA Covid doses.

To be clear, the finding does not provide definitive proof of genetic integration, or what researchers call “transfection.” For that, researchers must extract DNA from human cells and find the genetic sequences the vaccine delivers. How frequently the spike protein is appearing and whether the levels might have clinically significant consequences are also unclear.

The researchers have reported finding spike protein on conference calls with participants in their study in October and again this week. Two people independently told Unreported Truths of the study’s findings.

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Why Are We Giving Babies COVID-19 Vaccines That Don’t Work?

Despite persistent recommendations from U.S. health agencies to vaccinate children as young as six months against COVID-19, a new study led by the Centers for Disease Control and Prevention (CDC) found that the shots do not reduce the risk of SARS-CoV-2 infection in children under 5 years old and may actually increase the risk of infection in some children.

The study, published in a leading medical journal, analyzed data from three cohort studies conducted between September 2022 and April 2023 and found no difference in infection rates between vaccinated and unvaccinated children.

While health agencies claim that COVID-19 vaccines reduce the risk of severe disease in young children—who aren’t at risk for severe illness in the first place—the findings of this study show the shots do no such thing, which was a cornerstone of public health messaging during the pandemic.

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C19 HAS TAUGHT US DOCTORS DON’T UNDERSTAND HOW MEDICINES ARE MADE

If doctors did know how medicines are made, the SARS-CoV-2 injections would never have found their way into people’s arms.

Doctors would have shouted “Nine-months to develop and make an injection? Pull the other one, matey!”

In the world of medicines, the doctor is equivalent to the pilot of an aircraft, where passenger lives are in their hands. So it is with treating disease—patient lives are in doctors’ hands.

Could you imagine a pilot allowing his aircraft to take off, knowing it had been developed and made at least ten-times faster that ever before?

The manufacturer would need to explain in great detail what it had done differently to achieve such a miraculous outcome. Questions would be:

  • How were all the component parts designed and sourced so quicky?
  • How were manufacturing and supply contracts negotiated and signed-off so quickly?
  • How much testing were the wings, engines and other safety-critical components subjected to?
  • There are lots more, feel free to insert your own questions here…

The other thing, of course, is that the physical condition of the aircraft would undoubtedly give the game away. A wonky wing maybe, the odd bump in the fuselage, wires poking out from the cockpit?

A deathtrap for all to see…

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Following Japan, Europe Set to Approve Exotic New Self-Amplifying RNA ‘Vaccine’ Technology That May ‘Vaccinate’ Others Via Shedding

On Thursday the European Union’s medicine committee recommended marketing authorization of a novel exotic technology referred to as ‘self-amplifying RNA vaccines’ or ‘replicon vaccines’. Called Kostaive, it is reportedly for ‘protection’ against Covid. In October Japan became the first country on earth to begin injecting their population with the new shot.

“On 12 December 2024, the Committee for Medicinal Products for Human Use (CHMP) adopted a positive opinion, recommending the granting of a marketing authorisation for the medicinal product Kostaive, a vaccine intended for the prevention of COVID-19 in adults,” the European Medicines Agency said Thursday.

Unlike the notorious mRNA gene therapy injections used to ‘combat’ Covid, which make the vaccinated individual’s body produce an antigen (the spike protein in the case of the Covid shots) the new saRNA vaccines go a step further, making the body replicate the replication mechanism itself. Traditional (real) vaccines contain the antigen, which is intended to illicit an immune response in the body, unlike mRNA vaccines which make the body itself produce the antigen, which is then intended to illicit an immune response. Traditional vaccines also contain neurotoxins such as aluminum as an adjuvant (to agitate the immune system into action) and mercury as a preservative.

“Kostaive will be available as a powder for dispersion for injection. Kostaive is a RNA-based COVID-19 vaccine (ATC code: J07BN01). It contains a self-amplifying mRNA that encodes the SARS-CoV-2 spike protein. Self-amplifying means that the mRNA also carries instructions to make a protein called replicase. Once administered into a muscle, the replicase protein makes more copies of the mRNA, which the cell can use to make more spike protein. Vaccination with Kostaive induces the production of neutralising antibodies and a cellular immune response targeting the spike protein, which helps protect people against COVID-19,” the European Medicines Agency said Thursday.

The new shot triggers side effects 90 percent of the time.

“During the clinical trials for Kostaive, five deaths were reported among participants in the phase 3b study. Across study phases 1, 2, and 3a combined, 90 percent of injected participants experienced adverse events, with 74.5 percent reporting systemic reactions and 15.2 percent requiring medical attention after the first dose. Notably, many of the study authors are full-time employees of Arcturus Therapeutics, raising concerns about bias in their conclusions,” Lifesite News said Tuesday.

The new technology has been labeled as intrinsically dangerous and even as a bioweapon by some, sparking fears of the vaccine itself spreading to the non-vaccinated population, a step far beyond vaccine shedding.

“The man-made genes in the replicon vaccines, if introduced into humans, are likely to spread not only to other humans but also to other species,” The Expose said in September.

The novel vaccine technology is said to spread like a virus, vaccinating even those who refuse to take their shots.

“So this was a way to have a vaccine that spreads like a virus,” talkshow host Mike Adams said in a May 5, 2021 podcast. “And the research on this has been going on for over three decades.”

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How They Faked a Pandemic

In examining how the global response to COVID-19 unfolded, one cannot overlook the pivotal role of PCR testing. The very tool used to justify lockdowns, mandates, and “vaccines” was fundamentally flawed. Even the test’s inventor, Kary Mullis, warned that it was never meant to diagnose infectious diseases. Instead, it was weaponized to generate fear and compliance, creating what some call a “pandemic of PCR tests,” not an actual pandemic of disease.

PCR tests work by amplifying genetic material, doubling it with each cycle. With enough cycles—beyond the recommended 27—they can detect virtually anything. During the COVID-19 response, countries like Canada ran up to 43 cycles, yielding an overwhelming number of false positives. According to data from Germany’s Robert Koch Institute, these tests produced up to 86% false positives, leading to the illusion of widespread infection.

If we strip away the hysteria and false positives, the picture becomes clear: COVID-19 never approached the lethality or spread required to justify the measures taken. Respiratory infection peaks during 2019 and 2023 ranked higher in severity than the worst peaks attributed to COVID-19. What we faced was not a pandemic of disease but a carefully orchestrated narrative designed to justify unprecedented measures.

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They’re Trialing Self-Amplifying RNA-LNP-Based Products

On November 11, 2024, an article was published online in Business Wire pertaining to the launch of a clinical trial NCT06602531 intended to test “Safety and Immunogenicity Study of Self-Amplifying RNA Pandemic Influenza Vaccine in Adults.” 

Question: Why is the word “Pandemic” in the title? 

The article provides information on the ARCT-2304 product which is a “sa-mRNA vaccine candidate formulated within a lipid nanoparticle (LNP).”

So. Many. Questions. For example, beyond the use of the word pandemic in the study title, why is this product being called a vaccine? Why is a new version of a product riddled with unresolved compendial standard issues being trialed?

ARCT-2304 is a gene-therapy-based prodrug that uses self-amplifying RNA technology (specifically, the RNA-dependent RNA polymerase (RdRP) gene, which allows it to replicate autonomously) that originates from an Alphavirus. Just so you know, this makes these products genetically-modified organisms (GMOs) and this is because of the fact that the coding template is a modified Alphavirus genome with the virus sub-genomic bits spiked out and the foreign flu genes ‘spiked in.’ The genetic material is capable of reproduction. The following slide shows how they did this for the Covid-19 version (KOSTAIVE® (ARCT-154) Monovalent: JN.1). 

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VICTORY: Dr William Bay wins doctors’ right to criticise covid gene-vaccines

Friday marked the biggest victory yet for doctors against political persecution after the Queensland Supreme Court issued a scorching judgement against Australia’s medical regulators on Friday.

Queensland GP William Anicha Bay celebrated outside court after successfully overturning a politically motivated medical ban put on him for protesting against the covid gene-vaccines on safety grounds.

The Court did not enter into any debate about the safety of the controversial products but ruled only on whether the regulators’ decision or conduct was free from error.

The Medical Board of Australia suspended Dr Bay’s registration on August 17, 2022, less than three weeks after he accosted the Australian Medical Association (AMA) National Conference and asked the delegates to stop forcing the jabs on people in response to an infection where “there is only a 0.27 percent fatality rate”.

Dr Bay apologised for interrupting proceedings before saying the covid “vaccines” were killing people.

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There is no scientific definition of vaccine in US biological product law.

Reader question:

Is there a formal definition of vaccine in law?

My reply:

There is no scientific definition of vaccine in statute or regulation.

That’s why I urged Kirk Moore to ask DOJ to provide proof that what they supplied to his office was a vaccine.

DOJ can’t provide that proof, because the proof doesn’t exist.

Congress added the term ‘vaccine’ to the biological products law in 1970 for the first time but did not define the term or direct the executive agencies to adopt or promulgate scientific definitions in regulations.

There is a financial definition of ‘vaccine’ and a definition based on the design intention, adopted by Congress in 1987.

1987/12/22 – Congress and President Reagan passed Omnibus Budget Reconciliation Act of 1987, PL 100-203, 101 Stat. 1330, including Sec. 9201, Manufacturers Excise Tax on Certain Vaccines, to establish an excise tax on vaccines ordered and purchased by US government and manufactured by private companies, to fund the Vaccine Injury Compensation Trust Fund established in 1986.

This act is the only act through which Congress has ever defined the term ‘vaccine,’ defining ‘vaccine’ as “any vaccine (A) which is listed in the table contained in [26 USC 4131(b)(1)], and (B) which is manufactured or produced in the United States or which entered into the United States for consumption, use or warehousing.”

Congress in 1987 defined vaccine in the form that now appears at 26 USC 4132a(2) — “any substance designed to be administered to a human being for the prevention of 1 or more diseases” — but has never defined the term “vaccine” in physical, chemical or pharmacological terms, and neither has the HHS-FDA.

See Dean v. HHS, No. 16–1245V, 2018 WL 3104388, at * 9 (Fed. Cl. Spec. Mstr. May 29, 2018), cited in 86 FR 6249, HHS Final Rule, National Vaccine Injury Compensation Program: Revisions to the Vaccine Injury Table, “(defining ‘‘vaccine’’ as ‘‘any substance designed to be administered to a human being for the prevention of 1 or more diseases’’) (quoting 26 U.S.C. 4132(a)(2)).”

The lack of scientific definition for vaccine was reinforced/corroborated in 2011 by the US Supreme Court in Bruesewitz v. Wyeth, when the majority opinion stated at p. 13:

“Design defects…do not merit a single mention in the [1986 National Childhood Vaccine Injury Act] or the FDA’s regulations. Indeed, the FDA has never even spelled out in regulations the criteria it uses to decide whether a vaccine is safe and effective for its intended use.”

Justice Scalia did not write, but it is also true, that FDA has never spelled out in regulations the criteria it uses to identify a product as a vaccine.

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Will Congress Thwart RFK Jr.’s Data Audit and Recall of the COVID-19 Shots?

Congress’s December 4, 2024, Coronavirus Pandemic Report has inspired hope for justice in prosecuting US federal agencies and individuals who engaged in egregious acts of willful injury against Americans and global citizens (i.e. Dr. Anthony Fauci), while frequently citing 18 U.S.C 1001 (that it’s a crime to lie to Congress).

The Congressional report also ignited controversy amongst many members of the medical freedom movement. The major point of controversy comes from one bullet point on page-2 of Chairman Brad Wenstrup’s opening letter for the 557-page Subcommittee report.

“Operation Warp Speed was a tremendous success and a model to build upon in the future. The vaccines, which are now probably better characterized as therapeutics, undoubtedly saved millions of lives by diminishing likelihood of severe disease and death.”

This statement, combined with Trump’s and RFK Jr.’s recent Mar-a-lago meeting with the CEO’s of Pfizer, Eli Lilly, and PhRMA, are causing many health freedom leaders to contemplate if every current and even future government official of our federal, legislative and judicial branches under Trump is inevitably a “deep state operative.” Some medical freedom influencers continue to assert that we are simply watching more “good cop, bad cop theatre.”

A key question naysayers raise is, “Why would House Representative Wenstrup make a key point in the Coronavirus Pandemic Report be, ‘The COVID-19 vaccines undoubtedly saved millions of lives,’ unless everyone involved in the government, including Congress, were deep state operatives?”

Because Naysayers and Their Followers Only Read the 1st Two Pages of the 557-Page Report

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