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FDA Shuts Down Enquiries About DNA Contamination In Covid Vaccines

 The recent findings of DNA fragments in the Pfizer and Moderna Covid-19 vaccines has led many to question why the FDA, which is responsible for monitoring the quality and safety of the vaccines, has failed to sound the alarm.

For years, the FDA has known about the risk posed by residual DNA in vaccines.

"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."

The authors found "The presence of billions to hundreds of billions of DNA molecules per dose in these vaccines. Using fluorometry all vaccines exceed the guidelines for residual DNA set by FDA and WHO of 10 ng/dose."

The US Food and Drug Administration continues to insist that any residual DNA contamination in the Covid vaccines is not a problem and that it "Stands behind its findings of quality, safety, and efficacy for the mRNA vaccines."

"While concerns have been raised previously as theoretical issues, available scientific evidence supports the conclusion that the minute amounts of residual DNA do not cause cancer, or changes to a person's genetic code," added the FDA. The FDA would not provide the "Available scientific evidence" to support its claim, but it's worth noting that the vaccines' own product labels show that genotoxicity and carcinogenicity tests were not carried out prior to their use.

Instead, after months of enquiries, the FDA sent boilerplate responses to me saying, "With over a billion doses of the mRNA vaccines administered, no safety concerns related to residual DNA have been identified." 

https://brownstone.org/articles/fda-shuts-down-enquiries-about-dna-contamination-in-covid-vaccines/

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