Dr. Robert Malone jabs FDA for not addressing COVID-shot dangers

 December 27, 2023

This story was originally published by the WND News Center.

MRNA expert and COVID-19 shot skeptic Dr. Robert Malone has written in a column posted in the Epoch Times that the U.S. Food and Drug Administration is, in effect, gaslighting the American public about those shots.

The shots, not really vaccines because they are more like DNA treatment programs, have been the subject of government and employer mandates, and consumer skepticism, since they appeared during the COVID-19 pandemic, in which the deadly virus likely emerged from a Wuhan, China, lab doing experimentation on bat viruses and killed millions.

There have been those trying to pry information out of the government on those shots, including the Florida surgeon general.

But Malone explains the FDA "has clearly failed to establish that it was aware of the contamination or adulteration of COMIRNATY or SPIKEVAX final drug products with plasmid DNA fragments, and it has completely failed to insist on the testing necessary to establish dose-limiting toxicity of DNA fragments when delivered to animals or humans using these highly active lipid nanoparticle formulations."

He charged the FDA with a "lack of rigor" in responding to questions from the surgeon general, Dr. Joe Ladapo, regarding the "risks of this contamination."

In fact, he explained, originally in his own substack column, that the FDA responded to questions "with a series of statements that can be interpreted only as ignorant, incompetent, or intentionally misleading."

He said the residents of Florida deserve better "than to be misled" and gaslit about those risks.

Because of the lack of information, and more, he called for those products to be "withdrawn from the market until the necessary tests have been performed and safety demonstrated."

He cited the failure of government authorities to "identify and disclose DNA fragment contamination in the Moderna and Pfizer/BioNTech COVID shots.

He said Dr. Peter Marks of the FDA Center for Biologics Evaluation and Research has been the government official obfuscating the details.

"Experts from around the world have raised concerns about the safety implications of DNA fragment contamination in COVID gene therapy-based 'vaccine' products. Leading regulatory authorities have conceded that these rushed novel and complex biological products are contaminated and deliver both synthetically modified messenger ribonucleic acid (mod-mRNA) and a wide variety of uncharacterized shorter DNA fragments into the cells and tissues of those who have accepted these products," he warned.

"The Biden administration has previously mandated and currently markets these products in the United States for Americans of all ages, including during pregnancy, fraudulently claiming that they prevent SARS-CoV-2 infection and spread and COVID-19 disease and death."

He charged that the DNA fragments are "leftover contaminants from manufacturing the mod-mRNA 'payload.' The contamination was first detected and reported by experienced U.S. and Canadian genomic researchers, and their findings have been replicated by many other laboratories."

Malone, in fact, played key roles decades ago in developing mRNA treatments and came to prominence when COVID-19 hit the world.

Online biographies explained, "He's become a trusted source for people everywhere who aren't quite sure about these mRNA vaccines or whether they are really safe."

He previously served as a consultant to the government, and even a left-leaning description admitted that the mRNA treatments are "not perfect.'

That description admitted, "Some people do have severe, painful, and rare vaccine side effects."

Malone explained that Florida officials, including Dr. Ladapo, asked the FDA for information about how drugmakers evaluated the "risk of human genome integration or mutagenesis of residual DNA contaminants from the mRNA COVID-19" shots.

And other details.

The federal agency's response was posted online, but, he said, "failed to address the questions posed by the surgeon general, instead offering unsubstantiated platitudes such as 'safe and effective' combined with redirection to irrelevant and poorly documented information."

He suggested federal officials have a vested interest in the success of the COVID shots, as they have suggested the procedures be expanded to cancer treatments.

But he confirmed, "Worldwide administration of the resulting injectable products has been associated with more than 17 million excess deaths (globally) and large numbers of cases of heart damage (myocarditis) with a perverse predilection for young people, contradicting the repeated propaganda statement that these products are safe."

While government campaigns claim the shots "will enable herd immunity, will prevent infection, replication, and spread of SARS-CoV-2, and will also prevent COVID-19 disease and death," they actually "provide none of these benefits," he said.

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