COVID CRIMINALS | CRIMES AGAINST HUMANITY | MILLIONS OF DEATHS

The following crimes are well documented and undeniable.

Petty bureaucrats and drug companies unjustly discredited an inexpensive FDA-approved drug that would have prevented COVID-19 hospitalizations and deaths for political spite and financial gain. These perpetrators need to be held accountable for over 500,000 American deaths and the disruption of our economy.

Hydroxychloroquine, a safe and effective FDA-approved drug, was shown to prevent hospitalization if taken A.S.A.P. when early symptoms of COVID-19 . The drug is cost-effective at 60 cents per tablet with COVID-19 treatment consisting of 11 tablets taken over five days. The FDA considers HCQ to be a safer drug than Tylenol.

On March 24, 2020, Dr. Woodcock wrongly advises Bright that HCQ is a dangerous drug requiring a EUA (Emergency Use Authorization). Its use should be limited to hospitalized patients.

Instead of making hydroxychloroquine (HCQ) readily available to the general public for early treatment, as ordered, the FDA instead issued an EUA for for hospital use only.
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Bright and Dr. Woodcock promote this course of action, despite the early clinical data showing HCQ was the most effective in outpatients if given early during the initial infection, effectively eliminating hospitalization.

In a legal document, Rick Bright makes a blatant admission of insubordination to multiple layers of leadership, including the White House, HHS Secretary Azar, and Dr. Robert Kadlec, MD, the Assistant HHS Secretary for Preparedness and Readiness.
Bright states the following in his Whistleblower Complaint: “…instead of a Nationwide Expanded Access IND protocol. Implementing the EUA was a compromise position, to rein in HHS leadership’s initial campaign to make the drugs available to the public outside of a hospital setting“.

During a heated White House Situation Room meeting on April 4, 2020, Dr. Anthony Fauci MD, refused to consider the use of HCQ for COVID-19 treatment. He dismissed the ever-accumulating HCQ efficacy reports from China, South Korea, and France as simply “anecdotal.”

Dr. Fauci brushed off the accumulating evidence and diverts millions of federal funds into a program to test and manufacture an experimental drug named Remdesivir. Remdesivir must be administered via IV and can only in the hospital. Instead of early community treatment, as prescribed in the original pandemic plan. Dr. Fauci changed the plan to promote “Societal Lockdowns” and push the development of highly experimental mRNA vaccines by multinational pharmaceutical corporations.

On May 16, 2020 in Phase 1 clinical trials conducted by Gilead Sciences in cooperation with China and Japan, Remdesivir FAILED: It provided “no statistically clinical effect, with severe adverse reactions.”

On June 15, 2020 Dr. Fauci ignored the data that HCQ works if the drug is administered during the first five days of infection. The FDA falsely claims that HCQ is causing fatal heart rhythms in hospitalized patients when the COVID-19 virus itself is the cause. Hydroxychloroquine's EUA was revoked, despite the overwhelming evidence of its effectiveness.

On June 29, 2020 Dr. Fauci recommends a 1.6-billion-dollar purchase of Remdesivir despite the drug’s Phase 1 failure in China.

​On October 16, 2020, the WHO concludes that Remdesivir is an ineffective drug and does not recommend its use to treat COVID-19.

SOURCE https://www.thecompleteguidetohealth.com/thecovidcriminals.html