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DEVELOPING: Florida’s Surgeon General Joseph Ladapo Confirms Detection of DNA Fragments in COVID mRNA Vaccines

1LoverofGod

Well-known
The Florida Surgeon General, Dr. Joseph A. Ladapo, is demanding answers from Dr. Robert M. Califf, the Commissioner of the U.S. Food and Drug Administration (FDA), regarding the detection of host cell DNA fragments in mRNA COVID-19 vaccines developed by Pfizer and Moderna.
......On May 10, Ladapo sent a letter to Califf and former CDC Director Rochelle Walensky regarding the risks of the experimental COVID-19 vaccines.

The letter reads:
Your ongoing decision to ignore many of the risks associated with mRNA COVID-19 vaccines, alongside your efforts to manipulate the public into thinking they are harmless, have resulted in deep distrust in the American health care system. Beginning with Operation Warp Speed, and possibly to be continued with an additional $5 billion investment in Project NextGen, the federal government has relentlessly forced a premature vaccine into the arms of the American people with little to no concern for the serious adverse ramifications.
Data are unequivocal: After the COVID-19 vaccine rollout, the Vaccine Adverse Events Reporting System (VAERS) reporting increased by 1,700%, including a 4,400% increase in life-threatening conditions. We are not the first to observe such a trend. Dismissing this pronounced increase as being solely due to reporting trends is a callous denial of corroborating scientific evidence also pointing to increased risk and a poor safety profile. It also fails to explain the disproportionate increase in life-threatening adverse events for the mRNA vaccines compared to all adverse events.
In the letter sent last week, Ladapo raised alarms about potential nucleic acid contaminants in the Pfizer and Moderna COVID-19 mRNA vaccines, particularly those in combination with lipid nanoparticles and the identified Simian Virus 40 (SV40) promoter/enhancer DNA.
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Related:

by Dr. Robert Malone December 18, 2023 (Dr Malone is the inventer of the mRNA spike protein)

FDA Fails to Address DNA Adulteration Concerns​


Expert from article:


Despite the fact that the risks of DNA contamination with traditional cell-based vaccines are much lower than for the novel mod-mRNA lipid nanoparticle-based products, the cited FDA guidance documents include the following specific warnings concerning DNA contamination:

Residual DNA might be a risk to your final product because of oncogenic and/or infectivity potential. There are several potential mechanisms by which residual DNA could be oncogenic, including the integration and expression of encoded oncogenes or insertional mutagenesis following DNA integration.
In his response to the Surgeon General, Dr. Marks refers to a specific clause in this guidance to support safety of the levels of DNA fragment contamination, which in turn refers back to a WHO document. What he fails to acknowledge is that this guidance refers to DNA contamination in a directly injected (parenteral) vaccine, not one employing the most highly active DNA and RNA lipid nanoparticle delivery system ever devised by man. This oversight either reveals Dr. Marks’ profound ignorance of this significant difference (despite the Surgeon General having pointed this out in his initial letter), or a fraudulent attempt to gaslight and obfuscate the truth of the matter. Either ignorance or intentional cover up, hard to differentiate. Here is the cited clause:

You should limit residual DNA for continuous non-tumorigenic cells, such as low-passage Vero cells, to less than 10 ng/dose for parenteral inoculation as recommended by WHO (Ref. 31)
Reference 31 refers to.....

Complete article:

 
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