The Adulterated Covid Vaxxes By Brian Simpson

Dr Mary Beth Pfeiffer, “Adulterated’ Covid Vaccines Should Be Pulled from The Market: Experts,” comments on a story, which if we had a fair and honest mainstream media, not ultimately owned by Big Pharma, should have made headlines. The story relates to findings of DNA in vials of the mRNA vaxxes. The DNA contaminants, as foreign genetic material, could enter human cells, producing yet unknown ill-effects. Thus, at the Summit for Truth & Wellness conference Saturday October 21 in Rochester, N.Y., Dr Robert Malone said: “There are grounds for immediate pulling of the product. … Adulteration has always been one of the key parameters that would result in withdrawal of a product from the market.” Ryan Cole said: “It can permanently camp out.” “These little circles of DNA can stay within the nucleus. Every time that cell divides … it’s a problem. They’re adulterated. They’re contaminated.”

Stopping further mRNA Covid vaxxes is a good idea, but the added problem is that the horse has already bolted, and most of humanity has been vaxxed up. Excess deaths are being seen right across the West, and the big question is whether this is the final stages of the adverse effects of the vax, or just the beginning.   

https://rwmalonemd.substack.com/p/adulterated-covid-vaccines-should

“New findings of DNA in 27 vials of Pfizer and Moderna Covid-19 vaccines constitute a legitimate, indeed urgent, reason to pull the mRNA products from the market, experts on Covid vaccine science agreed in public comments at the Summit for Truth & Wellness conference Saturday October 21 in Rochester, N.Y.   

The presence of DNA fragments in the mRNA injections raises the unsettling prospect that a foreign genetic material, derived from E. coli, will enter and influence vaccinee cells in unpredictable and harmful ways. While the possible repercussions are unclear, such vaccine “adulteration” is itself an extraordinary breach of the manufacturers’ duty to report all components of vaccines for regulatory review, said members of an expert panel at the conference.  

“There are grounds for immediate pulling of the product,” Dr. Robert Malone, a virologist who worked in mRNA vaccination development, told a packed house of about 850 attendees. “Adulteration has always been one of the key parameters that would result in withdrawal of a product from the market.”  

The DNA revelations were posted in April on a pre-print server in Canada. On October 19, Health Canada confirmed what five researchers had found in every one of the tested vaccines—the presence of previously undisclosed sequences of DNA. In an email to Epoch Times, Health Canada, the equivalent agency to the CDC, acknowledged that “the sponsor [Pfizer] did not specifically identify the SV40 sequence" in preapproval documents. SV40 stands for Simian Virus 40, from which a DNA molecule was derived for use in Pfizer’s manufacturing process. 

FDA did not immediately respond to my request for comment. The agency did not directly address the DNA question from journalist Mary Ann DeMasi, after her September interview with Phillip Buckhaults, a cancer genomics professor at the University of South Carolina who independently replicated the findings. Instead, the agency assured her, "FDA is confident in the quality, safety, and effectiveness of these vaccines.”

The conference speakers, already universally concerned about deaths, myocarditis, blood clots, fertility issues and other post-vaccine events, detailed their concerns about the findings’ implications. 

Dr. Ryan Cole, an Idaho pathologist who early in the rollout spoke out on observed upticks in cancers, was troubled by this injected genetic material. “It can permanently camp out,” he said. “These little circles of DNA can stay within the nucleus. Every time that cell divides…it’s a problem. They’re adulterated. They’re contaminated.”   

 He said every state’s Attorney General, who bears responsibility for product safety, should be asked why they would allow a vaccine that is contaminated and “has unknown short-, medium- and long-term side effects.”  

DNA sequences were found in both Moderna and Pfizer vaccine products in amounts that are of concern, especially for people who receive multiple vaccinations. The Pfizer vaccine raises particular questions, since the SV40 DNA sequence was added belatedly in order to facilitate production of large amounts of DNA that in turn produce the RNA used in the vaccine. It was not disclosed to regulators, speakers said.

Pfizer’s initial vaccine trial, Cole and others said, involved 40,000 people who were given an mRNA vaccine manufactured in the original “process one.” When it proved cumbersome and impractical, the process was revised and the SV40-derived plasmid—a circular DNA molecule—was inserted. With that undisclosed change in the manufacturing process “comes a different risk,” Kevin McKernan, an author of the DNA study and former research manager for MIT’s Human Genome Project, said in a World Council for Health roundtable on October 16.

Warp Speed Failure

Naomi Wolf, co-founder of the Daily Clout, which has analyzed 450,000 pages of court-released Pfizer documents, was harshly critical of the new development, which she said fits a pattern of regulatory failure and unrecognized harms that have characterized the Covid vaccine rollouts. 

“This is a bait and switch,” Wolf told the audience, referring to the late-stage manufacturing process change. “We were told process one was going into our bodies, and then they rolled out process two.” 

Aided by some 3,000 volunteer reader-reviewers, the Daily Clout produced 83 reports in 21 months on the Pfizer documents. The effort found many so-called “signals” of harm—including 1223 deaths just in the three months of Pfizer vaccination campaign. 

Most recently, the project obtained heavily redacted high-level government emails indicating that officials were aware of vaccine-associated myocarditis early in 2021. “Instead of coming clean with the American people,” Wolf said, “they doubled down and came up with a strategy to cover it up.” 

 Referring to the process of assuring the safety and efficacy of such products, Wolf asked, “What happened to pharmacoviligence?” 

 Amy Kelly, the director of the Pfizer documents analysis, had an answer. Under Operation Warp Speed, FDA took just six weeks to scrutinize the trove of documents that her small army of people have taken months to scour.

“There’s just no way that [a thorough review] actually happened,” Kelly said. “There was not enough time for FDA to look at what was going on. The safety analysis wasn’t there.”  

‘Not hyper-alarmed’

In a telephone interview after the conference, David Wiseman, a vaccine expert and author of the DNA study, told me he agreed the vaccines should be withdrawn based on this new evidence. He also called on commentators to “tone down” their rhetoric surrounding it. “We want to know what damage was done over the last four years,” he said. “Is it a fraud? Adulteration? I have no idea. We need to have the right experiments.”

“Theoretically, everyone agrees that the DNA could be a risk for cancer,” he told me. “The question is, does the amount and type of DNA make that concern bigger or smaller.”