26% of those prescribed Remdesivir for COVID died, according to Medicare database

The high mortality rate and frequency of adverse effects associated with Remdesivir ‘begs the question … Why is this the protocol in American hospitals?’

It was after the FDA issued an Emergency Use Authorization (EUA) for the use of Remdesivir on May 1, 2020, that Ardis told the Corona Investigative Committee that America suffered the highest death rate from COVID-19 in the globe.

“Before May 10, the United States had a lower coronavirus death rate than other high-mortality countries, but after that date, all six of the other high-mortality countries (Belgium, France, the Netherlands, Spain, Sweden, and the United Kingdom) had lower death rates than the United States,” according to an October 2020 report from the Center for Infectious Disease Research and Policy (CIDRAP).

In addition, there was a continued failure to demonstrate any life-saving benefit of the drug. In October 2020, just before the FDA granted the drug final approval, a World Health Organization study found the drug didn’t decrease mortality or hospital stays.

Ardis has pointed out that a study on the “Compassionate Use of Remdesivir for Patients with Severe Covid-19” found that 60% of study patients reported adverse events, and 23% reported serious adverse events, the most common being “multiple-organ-dysfunction syndrome, septic shock, acute kidney injury, and hypotension.”

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