GOVERNMENT UNDERESTIMATES DNA CONTAMINATION IN VACCINES BY UP TO ONE HUNDRED TIMES (100x)

While other peer-reviewed studies have found lesser amounts of dangerous contamination, one peer-reviewed study has shown that in vials of modRNA vaccines made by Pfizer and Moderna, deoxyribonucleic acid (DNA) exceeded the regulatory limit set by the Food and Drug Administration (FDA) and the World Health Organization (WHO) by thirty-six times (36x), or more than three thousand percent (3600%), to one-hundred and fifty-three  times (153x), or more than fifteen thousand percent (15,300%), for Pfizer and by one hundred and twelve times (112x), or more than eleven thousand percent (11,200%), to six hundred and twenty-seven times (627x), or more than sixty-two thousand percent (62,700%), for Moderna.

But it’s even worse than that—while the contamination, along with the regulatory failure, is easily explained—since a recent preprint has found that methods recommended for testing by government regulators, as they are used by pharmaceutical companies, can substantially underestimate contamination.

These methods can be off by more than one hundred times (100x) or ten thousand percent (10,000%).

While he exposes regulatory failures, conflicts of interest, and weaponized retraction campaigns, the author has uncovered plasmid contamination within vaccine vials, including sequences, never disclosed to the regulators, of Simian Virus 40 (SV40).

That’s the stuff that was proven, more than twenty years ago, in peer-reviewed studies, to cause brain cancers, bone cancers, malignant mesothelioma, and non-Hodgkin’s lymphoma (NHL).

Vaccines are poison.

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