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?'
Shutterstock
Emily
Mangiaracina
Wed Sep 29, 2021 - 7:05 pm
EDT
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(LifeSiteNews) — An attorney
recently released data showing a remarkably high fatality rate for COVID
patients who were prescribed Remdesivir.
According to attorney Thomas
Renz, 25.9% of those prescribed Remdesivir
for COVID-19 are recorded as having died in the Centers
for Medicare & Medicaid Services (CMS) database. CMS data indicated
that of 7,960 beneficiaries prescribed Remdesivir for COVID‐19, 2,058 beneficiaries died. Forty-six percent of those
fatalities occurred within 14 days of Remdesivir treatment.
The death rate for COVID patients
prescribed Remdesivir dwarfs the fatality rate of COVID patients prescribed
Ivermectin, which is recorded by the CMS database as being 7.2%.
For the public’s further consideration of
Remdesivir’s safety, Renz has pointed out that a Remdesivir Clinical Trial
Final Report has shown that about a quarter of patients experienced
serious adverse events from the drug. The study, published in the New England
Journal of Medicine, showed that “serious adverse events were reported in 131
of the 532 patients who received Remdesivir (24.6%).”
Renz noted on his website that
this data “has been withheld by the government from our citizens.” He added,
“This begs the question … Why is this the protocol in American hospitals?
Does this appear ‘safe and effective’ to you?”
Remdesivir is currently the only Food and Drug
Administration-approved drug for the treatment of COVID-19, as
the COVID-19 Treatment Guidelines Panel continues to recommend
against the use of hydroxychloroquine, and will neither recommend for or
against Ivermectin.
In a presentation shared on his website, Renz also
pointed out that whereas hospitals will pay $390 per vial of Remdesivir, coming
out to an average of $2,340 to $3,120 for a five‐day course of
the drug, the average cost of Ivermectin per patient is $24.
Renz’s report of the CMS data is not the first to
find a high mortality rate with the use of Remdesivir. The drug was dropped
from a clinical trial for Ebola in 2018
after it was found that it had the highest death rate of the four drugs being
tested, Dr. Bryan Ardis shared in a videotaped interview by an international
legal group that is investigating human rights violations by governments during
the COVID-19 pandemic.
The Ebola clinical trial was sponsored by the
National Institute of Allergy and Infectious Diseases (NIAID), of which Fauci
is director. As one of then-President Donald Trump’s chief medical
advisers on COVID-19, he must have known that Remdesivir had a 50% death rate,
compared with 35% of two other drugs in the trial – and that serious
side effects, including at least one death, led to the drug being pulled
and research on it abandoned.
Even as Fauci promoted the use of Remdesivir for
the treatment of COVID-19 in April 2020, he admitted that “the mortality
benefit of Remdesivir” had “‘not yet reached statistical significance,’” as
CNBC reported.
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.”
Wolfgang Wodarg, a physician, politician, and
former head of the public health department in Flensburg, Germany, agrees with
Ardis that Remdesivir is “very toxic.”
“We don’t know any positive effect of this drug, we
only know toxic effects. So, this was for sure a wrong decision to give it to
so many patients with a positive PCR test,” Wodarg said in
a discussion on the
“mechanism of organ failure leading to the death” in 2020 of U.S. patients
diagnosed with COVID-19.”
TOPICS
Freedom
TAGGED AS
Centers For Medicare And Medicaid Services
Covid-19
Hydroxychloroquine
Ivermectin
National Institute Of Allergy And Infectious Diseases
Remdesivir
Vaccines
