Deadly Remdesivir

Dr. Vernon Coleman was one of the first doctors to point out that doctors are now one of the top three causes of death - along ...

Attorneys and Doctors Warn that Hospitals are No Longer Safe – Remdesivir Drug Kills 25% of Patients – 85% Patients on Ventilators Die

In this interview with Dr. Vliet, he gives an update on this work, and explains that the government's own data on Medicare/Medicaid treatments show that the Remdesivir drug kills 25% of patients who take it, and that 85% of patients put on ventilators for more than 96 hours end up dying.

He claims that this is purposeful and not an accident, as the people in the hospitals clearly know this is happening.

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Fauci’s Remdesivir Drug Fast-Tracked by FDA for Approval Exposed as a Fraud

Health Impact News

Del Bigtree’s Highwire program exposes how the new drug Remdesivir, developed by Anthony Fauci at the NIH, and fast-tracked for approval by the FDA, is a fraud, because clinical trials did not show it prevented deaths due to COVID-19, and may actually cause more deaths.

Fauci Hospital Protocol: Remdesivir Study…killing Patients

Saturday, September 11, 2021

Armed with Knowledge


While banning Hydrochloroqine and Ivermectin, Fauci, NIH, CDC mandates that hospital must use the Remdesivir protocol. This drug ,said to have been effective for Ebola, when reading the Ebola study on the CDC website reveals that it killed many of the subjects. Contaminated swabs, remdesivir protocol, faulty PCR test at high cycles, banning the cure (HCQ & Ivermectin), and telling the infected not to go to the hospital unless they we dying…that is…no early treatment allowed….. gave the illusion that Covid 19 was a deadly Pandemic

The post FAUCI HOSPITAL PROTOCOL: REMDESIVIR STUDY…KILLING PATIENTS appeared first on Vaccine Liberation Army.

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Stew Peters Proof: Docs Know They're Killing: Fauci's Deadly Remdesivir Had 50% Kill Rate in Ebola Trial! - Must Video

Monday, January 17, 2022

Remdesivir Increases Your Risk of Death. Dr. Paul Marik Speaks on the Deadly NIH Protocols and the Perverse Incentive Structure Driving this Mindless Approach in the Field.

January 25, 2022
Dr. Marik, Founder of the FLCCC, spoke Monday to Senator Ron Johnson’s Discussion Panel on the Deadly Approach to Covid-19 with Vaccine Mandates, Poisonous Protocols, and Restricted Therapeutics
“Dr. Paul Marik testifies about the dangers of remdesivir and the corruption in our medical system for prescribing it. Though it is deadly, doctors are being incentivized to use it on patients.
Remdesivir killed more than 50% of the animals during its clinical trials. Yet the FDA still approved it.”
– Covid Vaccine News – Telegram Find More Here: Telegram: Contact @CovidVaccineTruth

Dr. Paul Marik, FLCCC

See his full remarks here.

“Almost 850,000 poor souls have died. These have been unnecessary, needless deaths. The NIH Guidelines for the treatment of hospitalized COVID include Remdesiver and low-dose Dexamethasone. Consequently, almost every single patient in this country, in this country is treated with the combination Remdesivir and low-dose Dexamethasone.

The Palm Study Group investigated four drugs for the use of Ebola. The results were published December 12, 2019, in the New England Journal of Medicine. That date is particularly important because that signaled the beginning of Covid. The Data Safety Monitoring Board of that study terminated the study of Remdesivir. TERMINATED, because Remdesivir INCREASED THE RISKS OF DEATH AND RENAL FAILURE. It was SUCH A TOXIC DRUG the Data Safety Monitoring Board terminated the use of REMDESIVIR.

Yet, in January and February of 2021 the NIH, in the ACTT 1 Study, enrolled patients in a study looking at Remdesivir for the treatment of Covid-19. The last patient was enrolled April 19, 2020. Ten days later, before the study had actually terminated, Dr. Fauci sat in the Oval Office of the White House and he said, “The trial was good news.”

What Dr. Fauci did not tell you was that the primary endpoint of the study was changed half-way during the study. We all know, that is scientific misconduct. Because the study was not going to be positive, they changed the primary endpoint.

The original endpoint was an 8-point scale that included death and a requirement for mechanical ventilation. Knowing that Remdesivir would not affect those endpoints, they invented a bogus endpoint called, “Time to Recovery.” Which they showed, in this study, was statistically significant. And based on this bogus endpoint, Remdesivir was approved by the FDA on October 20th, 2020.

So, if one does a meta-analysis looking at the studies of Remdesivir, the two studies, which were sponsored by Gilead, show a reduction in mortality. However, if you look at the four independent studies, including the large study by the WHO, it shows the opposite effect. Remdesivir increases the risk of death. Let me say that again. Remdesivir increases the risk of death by 3%. It increases your chance of Renal Failure by 20%. This is a toxic drug.

But, just to make the situation even more preposterous, the Federal Government will give hospitals a 20% bonus on the entire bill, if they prescribe Remdesivir to Medicare Patients. The Federal Government is incentivizing hospitals to prescribe a medication which is toxic.

So, it should be noted that Remdesivir costs about $3,000 a course. Dr. Kory spoke about Ivermectin. Ivermectin reduces the risk of death by about 50%. It costs the WHO two cents. Two cents.

So as regards dexamethasone, this is the wrong drug, in the wrong dose, for the wrong duration of time. Yet, every clinician in this country will absurdly use this homeopathic dose of dexamethasone. Why?! Because the N I H tells them to do this.

So, what the NIH and other agencies have ignored are multiple FDA approved drugs. These are FDA approved drugs. These are not experimental drugs, which are cost-effective, and safe, and have unequivocally been shown to reduce the death of patients in ICU and in hospital.

For example, there are 25 high quality studies (some people complain about the quality of these studies – so if you select out the high quality, randomized controlled trials) they show that Ivermectin reduces the risk of death by 26%. This is an extremely safe and cheap drug. In fact, it is one of the safest drugs on this planet. You are more likely to die from taking Tylenol…..

(This is just to the 7-minute mark. There are 8 more minutes of truth left. Watch the video, see link.

Dr Mike Yeadon: Most Covid-19 Deaths were a direct result of the administration of Midazolam or Remdesivir

Wednesday, October 13, 2021

Most Covid-19 Deaths were a direct result of the administration of Midazolam or Remdesivir – By Dr Mike Yeadon


Listen Now

I often see Dr Anthony Fauci on TV or quoted in newspapers. So it seemed a good moment to outline the part of the story that I know about.

By Dr Mike Yeadon

Fauci is a ghastly inhuman person. Watch Kary Mullis’ last interviews. Scientifically, he drew a bead on Saint Fauci over the AIDS scandal. AZT (Wellcome) was a toxic drug from anti-cancer & immunosuppression research, being an analogue of the bases used in genetics.

Politicians BREACH The Declaration on Bioethics and Human Rights and Nuremberg Code Left, Right and Center

Crimes Against Humanity Committed in Gibraltar – Christ demands that the RGP Commissioner and Governor Arrest and Prosecute the Perpetrators

CRIMES AGAINST HUMANITY – Dr. Reiner Fuellmich, his bombshell videos, and the legal-suits

GRAND JURY - The court of public opinion

January 21, 2022

FDA Approves Veklury® (Remdesivir) for the Treatment of Non-Hospitalized Patients at High Risk for COVID-19 Disease Progression

-- Approval Based on Phase 3 Data Showing Veklury Significantly Reduced Risk of Hospitalization By 87% Compared with Placebo --

-- NIH Guidelines Recommend Veklury for the Treatment of Non-Hospitalized Patients at High Risk --

-- FDA Expands Pediatric Emergency Use Authorization (EUA) to Include Treatment of Non-Hospitalized Pediatric Patients at High Risk --

In the United States, Veklury is indicated for the treatment of COVID-19 in adults and pediatric patients (12 years of age and older and weighing at least 40 kg) who are either hospitalized or not hospitalized and are at high risk for progression to severe COVID-19, including hospitalization or death. Veklury is additionally authorized for these uses under the EUA for pediatric patients weighing 3.5 kg to less than 40 kg or pediatric patients less than 12 years of age weighing at least 3.5 kg. Veklury is contraindicated in patients who are allergic to Veklury or any of its components; please see below for additional Important Safety Information for Veklury.

Watch the Water

I’m not sure if this has been posted? It would seem appropriate that snake venom has played a part in all of this.

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@jeremy ,


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Remdesivir ‘Disastrous’ as COVID Treatment, But Government Pays Hospitals to Use It

So far, all of the drugs developed against COVID-19 have been disastrous in one way or another. Remdesivir, for example, which to this day is the primary COVID drug approved for use in U.S. hospitals, routinely causes severe organ damage, and, often, death.

Despite its horrible track record, the U.S. government actually pays hospitals a 20% upcharge for sticking to the remdesivir protocol, plus an additional bonus. Hospitals must also use remdesivir if they want liability protection.

Incentives like these have turned U.S. hospitals into veritable death traps, as more effective and far safer drugs are not allowed, and hospitals are essentially forced to follow the recommendations of the U.S. Centers for Disease Control and Prevention.

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Dangerous Deadly Remdesivir - another spot in a row here - now by Dr Ardis - Nebezpecny Smrtici Remdesivir - dalsi spot v rade - nyni od Dr Ardise

FAUCI EXPOSED: Charlatan, Fraudster, Profiteer

The Whole Pandemic Was A TROJAN HORSE For Vaccines – Fauci Is The Epitome Of Evil

Dr. David Martin – The Vax is a Bioweapon; Call it what it is.

GRAND JURY - The court of public opinion

09/13/22 - 3:00 PM

Fresno, CA — Remdesivir Deaths Lawsuit Press Conference


Three California hospitals being SUED for administering “remdesivir protocol” to patients without informed consent, resulting in DEATH

Tuesday, September 13, 2022 by: [Ethan Huff]

The controversial antiviral drug, which padded the pockets of Tony Fauci and others throughout the plandemic, is extremely deadly and does not provide any protection against the Fauci Flu. The drug has been linked to kidney damage, resulting in more hospitalizations and early deaths than if it was never used at all.

Covid patients at the three aforementioned medical facilities in Fresno were administered what the complaints describe as a “remdesivir protocol.” They received “uninformed consent,” the complaints explain, meaning they really had no choice in the matter and were simply told that this was the established remedy for Chinese Germs.

The three-complaint lawsuit was unveiled at an event called “Remdesivir Death: Landmark Lawsuit,” which was attended by supporters such as Dr. Peter McCullough, Dr. Bryan Ardis, Dr. Angie Farella, and Dr. Janci Linsay. Each of these individuals has spoken out in the past about how remdesivir is dangerous and should not be used to treat patients.

At least 14 Fresno-area families are named as plaintiffs in the suit. They say that the three hospitals being sued engaged in medical deception and failed to provide informed consent, as is required by law, before exposing patients to the deadly drug cocktail.

“Full informed consent means that patients must be provided with full information about the deadly harm that this dangerous experimental drug causes on its own,” the lawsuit states. “They must be told that the only time it was ever tested, it was pulled because it killed so many people.”

NEJM study finds remdesivir to be least effective, most deadly pharmaceutical “remedy” for covid

Also referenced in the lawsuit is a study published in the New England Journal of Medicine (NEJM) which found that of the pharmaceutical drug candidates evaluated for the Chinese Virus, remdesivir was found to be the least effective and most deadly option.

Even so, the National Institutes of Health (NIH) under former head Francis Collins claims that remdesivir is the only drug currently approved by the U.S. Food and Drug Administration (FDA) to treat the Fauci Flu.

“Remdesivir received Emergency Use Authorization in or around May of 2020, after being recommended by an NIH panel that contained nine individuals with financial ties to its creator, Gilead Sciences,” the lawsuit adds. “It is very nearly the equivalent of a death sentence for a COVID patient, or a patient with real Pneumonia (as opposed to ‘covid pneumonia’).”

What this means, according to the lawsuit, is that the three hospitals in question violated the Nuremberg Code by engaging in medical experimentation on patients without informed consent. This is a serious violation, representing crimes against humanity that must not go unpunished.

In some of the cases mentioned in the suit, patients were given remdesivir even after they explicitly declined the protocol. This amounts to forced drugging and pharmaceutical assault.

“A patient comes to the hospital often for a problem unrelated to COVID-19,” the suit explains further. “They are told they have COVID-19 or ‘COVID pneumonia.'”

From there, patients are separated from loved ones and placed in a room where the only option available to them is remdesivir.

They are placed on a BiPap machine at a high rate, making it difficult for them to breathe,” the lawsuit adds. “Their hands are often tied down so they can’t take the BiPap machine off their face.”


‘Friday Roundtable’ Episode 28: Vaccine-Related Aluminum Exposure Linked to Persistent Asthma, Remdesivir Deaths Lawsuit + More

](‘Friday Roundtable’ Episode 28: Vaccine-Related Aluminum Exposure Linked to Persistent Asthma, Remdesivir Deaths Lawsuit + More - Friday Roundtable - CHD TV: Livestreaming Video & Audio)

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Patients died from COVID-19 drug treatment at Redlands, Riverside hospitals, suits allege

'We are helping victims to raise public awareness and hold the physicians and hospitals accountable for this atrocity,' says the plaintiffs' attorney.

Two women have filed lawsuits alleging their husbands died from negligence at Inland Empire hospitals after doctors prescribed remdesivir to treat COVID-19 and then failed to tell them about dangerous side effects of the anti-viral drug.

The lawsuits, filed last month in state court against Kaiser Permanente Riverside Medical Center and Redlands Community Hospital and several of their physicians, allege doctors engaged in fraud by prescribing each of the men remdesivir without their knowledge or consent. Doctors also allegedly failed to explain that the drug is ineffective in treating COVID-19, is toxic to kidneys and can cause death, the complaints say.

“In COVID-19 healthcare circles across the country, remdesivir has carried the nickname ‘Run, death is near,’ ” said the civil complaint, which seeks unspecifed damages. “Remdesivir is medically unnecessary for treatment of COVID-19.”

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Protocol Remdesivir kills

Deadly Remdesivir kills the kidneys

From video:
Who knows what they are putting in people; three main jabs going out; a placebo, designed to deceive, allowing those who had it to tell others nothing happened to them, then the clot shot, jelly clots are huge playing out right now is the one that destroys the immune system.

Freedom warriors Jacqui Deevoy, John O'Looney and Matt Le Tissier

Remdesivir estimated to have killed 100,000 Americans

By Rhoda Wilson on March 15, 2023
John Beaudoin is calling for a criminal investigation into remdesivir citing data that it may have killed 100,000 people in America.

The US Food and Drug Administration (“FDA”) authorised the experimental antiviral drug remdesivir, brand name Veklury, for emergency use against covid-19 in May 2020. By October 2020, it had received full approval. It remains a primary treatment for covid-19 in hospitals, despite research showing it lacks effectiveness and can cause high rates of organ failure.

In mid-February, Beaudoin called for a criminal investigation into the drug, citing data for Massachusetts he estimates remdesivir may have killed 100,000 people in the US. “They know,” he tweeted, “or they wilfully refuse to know. Either way, it’s homicide.”

Remdesivir Thread – 47 sec Video first followed by Massachusetts graphs.
Estimated 100K people were killed by Remdesivir in USA alone. They know or the willfully refuse to know. Either way, it's homicide.

— John Beaudoin, Sr. aka, Coquin de Chien (@JohnBeaudoinSr) February 13, 2023

Using a Freedom of Information Act (“FOI”) request, Beaudoin received all the death certificates in Massachusetts, USA, from 2015 to 2022. He produced graphs from the information he received and found 1,840 excess deaths from acute renal failure from 1 January 2021 to 30 November 2022, which he believes may be due to remdesivir.

Beaudoin also revealed an increase in deaths from acute renal failure (“ARF”) in every age group over 15 years old, from 2015 to 2022. “Thousands dead in Massachusetts ARF likely due to remdesivir. This requires CRIMINAL investigation,” he tweeted attaching the graph below.

Remdesivir was developed by Gilead Sciences. The first shipments of remdesivir into the US were received in May 2020. At the time, according to Gilead’s website, it was “not known if remdesivir is safe and effective for the treatment of covid-19.”

Scientists who had closely watched the clinical trials of remdesivir unfold over the 6 months leading up to an agreement signed to supply remdesivir to the European Union (“EU”) and the FDA’s full approval for covid in October 2020 were baffled by both decisions. They had many questions about remdesivir’s worth.

One large, well-designed study found remdesivir modestly reduced the time to recover from covid in hospitalised patients with severe illness. A few smaller studies found no impact of treatment on the disease whatsoever. Then, on 15 October 2020 – in decidedly unfavourable news for Gilead – the fourth and largest controlled study delivered what some believed was a coup de grâce: The World Health Organisation’s (“WHO’s”) Solidarity trial showed that remdesivir did not reduce mortality or the time covid patients took to recover.

As reported by Science both FDA’s decision and the EU deal came about under unusual circumstances. Read more HERE.

On 20 November 2020, WHO issued a recommendation against the use of remdesivir in hospitalised patients, regardless of disease severity, as there was no evidence that remdesivir improved survival and other outcomes.

On 22 April 2022, WHO changed its recommendation following the publication of data from “a,” one, clinical trial. WHO’s updated recommendation is that remdesivir can be used in mild or moderate covid patients who are at high risk of hospitalisation.

Dr. Paul Marik, a pulmonary and critical care specialist and founding member of the Front Line Covid-19 Critical Care Alliance, explained that during the pandemic the only drug he was allowed to prescribe was remdesivir and that remdesivir increases the risk of kidney failure 20-fold.

During a roundtable discussion held by Sen. Ron Johnson on 7 December 2022 titled ‘Covid-19 Vaccines: What They Are, How They Work and Possible Causes of Injuries’ Dr. Marik said:

“We know, according to the WHO, remdesivir increases your risk of kidney failure 20-fold. Remdesivir will increase your risk of developing renal failure 2-fold. It increases your risk of dying by about 4%. It has no place in medicine. Yet the Federal Government will give hospitals a 20% bonus on the entire hospital bill if you prescribe this toxic [and ineffective] medication. So, you can see how the hospitals and health care systems are now subservient to industry rather than doing what’s best for their patients.”

Criminal Investigation for Remdesivir Caused Excess Deaths, Dr. Joseph Mercola, 10 March 2023