FDA Finally Beginning to Link Children’s Deaths to mRNA Vaccines

BY JEFF SKINNER 

STATEWIDE - In a memo recently released to the public over the Thanksgiving weekend, current FDA head of the Center for Biologics Evaluation and Research, Dr. Vinay Prasad, has admitted there is a direct link between the Covid-19 injections and the death of children who received them, and theorized the CDC and FDA may have been aware and silent about it during the rollout.

While this revelation may not be new to readers of TOR and its associates, as we have covered the mechanism of action for the mRNA injections and how they could lead to death in healthy individuals, a decrease in fertility, miscarriage and stillbirth. That said, this is the first time an official government organization is admitting a causal link. Though the memo from Prasad is careful to only link 10 infant deaths directly to the mRNA injection, it takes the deaths as a warning signal, which Prasad goes on to theorize it should have been difficult for the former CDC director, Rochelle Walensky, to ignore. Further, the memo admits there are likely much more that the previous CDC and FDA overlooked and waited on discussing until the drug could be brought to market for the age groups it likely killed. 

“Prior to joining the US FDA, the FDA Commissioner closely followed reports of vaccine-induced myocarditis. Unlike the COVID virus, which has a steep age gradient– being at least 1000 times more likely to kill an 80 year old than an 8 year old– myocarditis appeared to have the opposite pattern. Young, healthy boys and men– those least likely to experience bad covid outcomes– bore the greatest risk. The risk was as high as ~200-330 per million doses given in the highest risk demographic groups. Notably, the US FDA and CDC were not the first to recognize the safety signal– instead the Israelis were– and worse in May of 2021, then CDC director Rochelle Walensky stated, “We have not seen a signal and we’ve actually looked intentionally for the signal in the over 200 million doses we’ve given,” Many felt this statement was dishonest and manipulative. 

"The Commissioner, senior advisor Tracy Beth Hoeg MD PhD, myself and colleagues demonstrated that COVID-19 boosters, and the accompanying mandates by colleges, were on balance harmful to young men in a widely discussed, peer reviewed paper in 2022. Like many academic physicians, we felt the FDA and CDC abdicated their duty to the American people. These agencies did not quickly attempt mitigation strategies such as spacing doses apart, lowering doses, omitting doses among those with prior COVID-19. 

Worse, the FDA delayed acknowledgement of the safety signal until after it could extend marketing authorization to younger boys 12-15. This is described by the Commissioner and I in JAMA. Had the acknowledgement come early, these younger boys, who likely did not require COVID-19 vaccination, may have chosen to avoid the products.”

As many may remember, warnings were being screamed out on social media by healthcare professionals, doctors with specialties in the field of gene technology and virologists, all stating the mRNA injections were incredibly lethal and failed to even offer the basic level of protection against the respiratory virus they claimed. In fact, even insurance companies like OneAmerica stated their metrics indicated a 40% increase in all cause mortality death from working age adults.

Given the level of studies, warning signs and explanations by experts which predated the release of the vaccines, rollout of and post analysis, the failure of the FDA and CDC to adequately evaluate and warn citizens of the risks, and it some instances even being complicit in coverup, would constitute a violation of  Section 335b(a)(1) of the FDCA by Making false statements or misrepresentations of a material fact, specifically from former CDC and FDA heads. Additionally, the move would constitute Conspiracy to defraud the government or the public.

There is no indication from the memo that any further action will be taken by the DOJ or FBI to investigate connections between the regulatory agencies and the pharmaceutical companies that benefited from the silencing of victims. 

The complete emailed memo is posted below.