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Mike in the Night E522 , Next Weeks News Today , Call ins , Lets Talk Fixing this Mess

The recently authorized Wuhan coronavirus (COVID-19) "booster" shots, promoted by the Biden administration, have been given the green light by the U.S. Food and Drug Administration (FDA) without any supporting clinical trials. Dr. Robert Malone criticized the FDA's decision, stating that the agency has acted recklessly and disregarded its own standards of integrity.

During an appearance on EpochTV's "Crossroads" program on September 11, the day of the FDA's approval, Dr. Malone strongly criticized the agency for abandoning its commitment to honesty and integrity.

Dr. Malone emphasized that there is insufficient clinical trial data, especially in human subjects, to justify the approval and emergency use authorization (EUA) of these new COVID booster shots by the FDA.

The FDA's justification for the shots is based on the assertion that it possesses adequate evidence from non-clinical trials, citing "neutralizing antibodies as detected in mice and their cross-reactivity as indicative of protection."

Dr. Malone firmly refuted this claim, stating that it is false, as there are no established markers of protection for SARS-CoV-2.

(Related: Dr. Malone previously noted a significant increase in life insurance claims following the initiation of Operation Warp Speed last year.)

The recent approval and emergency use authorization (EUA) of the Pfizer and Moderna Wuhan coronavirus (COVID-19) "vaccines" by the Food and Drug Administration (FDA) have been met with widespread public dissatisfaction, and this sentiment is well-founded. These shots have not undergone proper testing and are considered unsafe.

In a surprising turn of events, Newsweek, which had previously advocated for the incarceration of the unvaccinated, is now criticizing the FDA for endorsing these so-called "vaccines" without conducting any human clinical trials. According to the report, the new "booster" shots (or whatever they may be termed) were only tested on eight mice. This level of experimentation falls far short of acceptable scientific standards.

Nick Mordowanec from Newsweek points out, "These updated boosters will be the first released to the public without any humans involved in the clinical trials, raising questions from some about the efficacy."

It's worth noting that in June, the FDA itself urged Pfizer and Moderna to develop these new shots, claiming that a new variant of COVID-19 would emerge in the fall that the earlier shots would not effectively cover. This led to the development of the additional jabs we now have available.

Mandy Cohen, director of the U.S. Centers for Disease Control and Prevention (CDC), emphasized, "We have more tools than ever to prevent the worst outcomes from COVID-19," in reference to the new jabs requested by the FDA and now in circulation.