Deadly Remdesivir

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 ,

TWT

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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

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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

https://www.stewpeters.com/video/2022/12/wuhan-whistleblower-tells-all-new-evidence-covid-19-man-made-in-u-s-lab-dr-fauci-exposed/

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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

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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. pic.twitter.com/5jDhPho7gf

— 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

RFK Jr: "Tony Fauci Knew That Remdesivir Would Kill You"

image

RFK Jr.:

"Fauci knew that Remdesivir would kill millions because just two years prior he had overseen a study in which it killed 54% of patients."

“In 2019 he tried to use it for Ebola and within five days of treatment in gave lethal side effects for 54% of the people. The safety monitoring ward ordered him to terminate the use of that drug. And he threw a phony, contrived, absolutely fraudulent study that he manipulated and orchestrated of that drug."

"It is homicide.”

LancetGate: “Scientific Corona Lies” and Big Pharma Corruption. Hydroxychloroquine versus Gilead’s Remdesivir

The Battle to Suppress Hydroxychloroquine as a Cheap and Effective Drug for the Treatment of Covid-19 By Prof Michel Chossudovsky

Global Research, March 15, 2023
Since this article was first published almost three years year ago on July 11, 2020 under the title LancetGate: “Scientific Corona Lies” and Big Pharma Corruption. Hydroxychloroquine versus Gilead’s Remdesivir on July 3, 2020, there has been a virtual censorship of debate on Hydroxychloroquine (HCQ) and Ivermectin largely directed against medical doctors.

In recent developments Remdesevir is making the headlines. Remdesevir is now approved for babies.

On May 22, 2020 Remdesivir for the Treatment of Covid-19 — Preliminary Report by National Institute of Allergy and Infectious Diseases, National Institutes of Health, was published by the New England Journal of Medicine, (NEJM)

On June 29, 2020, Dr. Anthony Fauci, who is the head of NIAID granted the “Greenlight” to Gilead Sciences Inc. despite the fact that the study of the new experimental drug was “preliminary”.The NIH-NIAID sponsored report (May 22) was used to justify a major agreement with Gilead Sciences Inc.

A $1.6 billion agreement between the HHS and Gilead Sciences Inc. was announced on June 29th, 2020 despite the fact that NIH NIAID study published in the NEJM was considered “preliminary”. In the late 1990s, Gilead Sciences Inc was headed by Donald Rumsfeld (1997-2001), who later joined the George W. Bush administration as Secretary of Defense (2001-2006).

In recent developments, there is an ongoing campaign to suppress both Hydroxycholoroquine as well as Ivermectin as effective preventive and curative drugs.

*The objective has been to sustain the vaccination campaign on behalf of Big Pharma.*LancetGate: "Scientific Corona Lies" and Big Pharma Corruption. Hydroxychloroquine versus Gilead's Remdesivir - Global ResearchGlobal Research - Centre for Research on Globalization

America is Led by Murderers – What Can Citizens Do?July 30, 2020


Dr. Anthony Fauci is employed by the United States government in the National Institute of Health. He is not an elected official, and has been in office for 38 years during the tenure of 6 presidents, and probably has more power than the Office of the President of the United States. Is he “untouchable?”

Commentary by Brian Shilhavy
Editor, Health Impact News

There is overwhelming evidence that Dr. Anthony Fauci, the director of the National Institute of Allergy and Infectious Diseases since 1984, is guilty of mass murder.

Earning huge profits from the pharmaceutical industry, he has been the main leader in the United States controlling the Coronavirus response, which has included squelching public information about hydroxychloroquine, a safe FDA-approved drug which has been in the market for decades, and which thousands of doctors are now saying has a 100% cure rate for patients diagnosed with COVID-19.

This action alone has led to tens of thousands of needless deaths, as well as billions of taxpayer dollars spent on “new” cures for COVID-19, such as the very profitable Remdesivir, and the upcoming COVID vaccines.

He seems to wield more power and influence than even the President of the United States.

So is there no way to stop him or bring him to justice?

American Citizens vs. the Wall Street Central Bankers

What Dr. Fauci and others like him who are complicit in mass murder has is unlimited financial resources, as he is part of the Wall Street Central Bankers who pretty much control the affairs of the world through International organizations such as the World Health Organization, the World Economic Forum, the Council on Foreign Relations, and many other organizations that are linked to Central Bankers.

What allows this small group of Billionaires to control the affairs of the world and get away with mass murder is not their wealth, however, but a compliant and non-resistant citizenry.

An uprising among the “common folk” is what they fear most, because the “common folk” outnumber them significantly, and it would not even take a majority of the “common folk” to overthrow their power.

They use subtle mind-control techniques to control narratives, and they also use the media, and especially today in the 21st Century, they use Big Tech to squelch freedom of thought and expression.

They keep the masses fighting each other instead of them, by creating political and social divisions that the masses in large part do not even understand originate from this small group of wealthy people.

And when you get to the top of the power structure of these people, you will see they are not very nice people at all. They are very evil. They are Satanists who are involved in the Occult and they are pedophiles and murderers. To learn more about this, see:

Unmasking Who is Behind the Plandemic and Rioting to Usher in the New World Order

What Can Citizens Do? (Return to God's Law)

The political system in the U.S. is thoroughly corrupt. Our Constitutional principles, originally drafted and implemented to protect citizens against the over-reach of a tyrannical government, pretty much died in 1913 when the Federal Reserve Bank was setup to control the monetary system.

Bankers and Wall Street have pretty much ruled the nation ever since then. They control the Presidency, the Congress, and the Supreme Court.

Here are a couple of suggestions I have today, here in July of 2020, of how citizens could potentially take back the country away from the powerful bankers and Wall Street.

Petition to the Gibraltar Parliament Demanding the Return to God’s Law

Shocking Ruling: Judge Denies Immunity to Maker of Remdesivir Under PREP Act After Man Suffers Severe Injuries

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Do you know how long people injured by COVID-19 drugs like Remdesivir and Paxlovid and people suffering from devastating vaccine injuries have been trying to get around the blanket immunity our government gave pharmaceutical companies under the Public Readiness and Emergency Preparedness (PREP) Act for the harms caused by their products?

Years.

Continued at link.

Thank-You for the Good news. Hopefully this is the beginning of the tide turning with many more Judges following these two Judges right decesion to deny immunity for such heinous crimes against humanity.

They knew they were giving this man glass particles in the Remdesivir?

Taken from article above: St. Joseph Mercy Chelsea Hospital and Gilead claimed they could not be sued because they had immunity under the PREP Act. Both the pharmaceutical company and the hospital attempted to get the case dismissed.

Apparently, Gilead thought that when the U.S. Food and Drug Administration (FDA) approved its drug, it also approved the glass particles that mysteriously ended up in as many as 55,000 doses of their product.Johnson said he knew it would be an uphill battle, but he is proud of both judges [in state and federal court’] who reviewed the case and saw through the charade—that Gilead Sciences Inc. got approval for the drug but not the glass particles that contaminated its vaccine.

Now because of this crime against humanity Mr.Johnson, whom once healthy requires 24/7 care by his family due an extremely horrific, unthinkable act, knowingly done to him, the glass particles were there in the Remdesivir, by St. Joseph Mercy Chelsea Hospital and Gilead.

Drug manufacturer, hospital immunity denied

# Drug manufacturer, hospital immunity denied

Hospitals are Prisons

HOW HOSPITALS ARE KILLING US - MANY BOOMS!

Dr. Vernon Coleman - How Hospitals Have Become Death Camps; MDs And Nurses Are Murderers

Health officials claimed remdesivir would stop COVID-19 — instead, it stopped kidney function, then blasted the liver and other organs. So why did the U.S. Food and Drug Administration approve the drug for people with kidney disease?

Covid Related News: SA court orders covid vaccine contract to be made public and US court rules manufacturer and hospitals liable for remdesivir injuries

By Rhoda Wilson on August 21, 2023
Results of contaminated DNA in Pfizer’s covid injections have been replicated and confirmed. This is just one of many dangers of injecting synthetic DNA into humans.

Vaccine victims of the first bout of covid injections is being ignored while corporate media ramps up the fear to get people to roll up for another round. The corporate media hype from the UK and USA about a new covid variant has now infected corporate media in Germany.

A high court in South Africa orders the government to make covid “vaccine” contracts and related documents public.

Families of four people who died from covid are suing EcoHealth Alliance for funding and releasing a bioweapon known to be capable of causing a worldwide pandemic.

A judge ruled in Michigan that the manufacturer of remdesivir and the hospital that used it are not protected by law if a patient is injured by its use. Below is a collection of articles from recent days from a variety of sources.

A true account of covid in Israel: In the imaginary world of Haklai et al. nothing ever goes wrong, as far as covid is concerned. There is no misclassification of deaths, there are no biases that distorts estimates of vaccine effectiveness, and there are no deaths due to the disruption of normal life. Too bad their data provide evidence to the contrary. Read more HERE.

The vax-gene files; have the regulators approved a trojan horse? Kevin McKernan’s results – for the Pfizer covid “vaccine” – have now been independently verified by a number of internationally recognised laboratories confirming both the presence and levels of DNA contamination across different vials and batches.

Levels of DNA contamination in the Pfizer BNT162b2 product came in around 18-70 times over the limits set by regulatory authorities. These levels of contamination have also been confirmed independently. Subsequent experiments suggest that most of the DNA contamination is fragmented, which is by no means benign.

We have DNA, which is mostly packaged in LNP designed to travel all over the body and enter cells, delivering it’s genetic cargo like a trojan horse. Some of this DNA may contain the SV40 promoter sequence – the one known to make a beeline to the nucleus and turn on gene expression. McKernan states an obvious concern, “If (the SV40 promoter) becomes integrated into the genome it will turn on gene expression wherever it lands. If this happens to be an oncogene (a cancer-causing gene), you’ve got problems.”

This, dear reader, is only one of the many possible adverse effects from injecting synthetic DNA into humans. Read more HERE.

Vaccine victims with no voice: While the pharma companies and medical authorities have profited from every dose of covid “vaccine,” the injections have injured countless people irreparably and destroyed the lives they knew. The media will not give voice to these injured whose ranks grow daily. Here we share some of their stories. Read more HERE.

Covid mRNA vaccine injury treatment: Curcumin (turmeric) blocks spike protein (combine it with bromelain), treats myocarditis, and has anti-inflammatory, anti-ageing and anti-cancer properties. Dr. William Markis has written about mRNA vaccine treatments: NATTOKINASE, QUERCETIN, N-Acetyl CYSTINE (NAC), OLIVE LEAF, BLACK SEED/NIGELLA, BROMELAIN and 3-DAY FASTING. Now he writes about curcumin. Read more HERE.

Eris vaccine marketing hits Germany: “Eris” and “Fornax” are the names given to two “subvariants” of something for which it is claimed both a new Moderna and a new Pfizer “covid vaccine” is effective against, Reuters reported on Friday. Eris is the nickname for EG.5 which WHO has labelled a “variant of interest.”

We will not be free of the virus until we are free of the vaccinators. Eris vaccine marketing via corporate media had already hit Germany on Sunday, complete with panic about a non-existent August “covid wave” ripped from British and American headlines. Despite all the obnoxious verbiage from corporate media, absolutely nothing of virological note is happening in Germany. Read more HERE.

Landmark win in South Africa for transparency of covid contracts: Several civil society organisations fighting for transparency in the procurement of covid vaccines by the South African government celebrated on Thursday after the Gauteng Division of the High Court in Pretoria ordered that the country’s vaccine contracts and related documentation be made public. Read more HERE.

Covid victims’ families sue Ecohealth Alliance for “funding, releasing” virus: The families of four people who died from covid are suing EcoHealth Alliance, the New York-based non-profit that was conducting gain-of-function research on bat coronaviruses in Wuhan, China, before covid broke out across town. According to the 2 August lawsuit filed before the New York Supreme Court in Manhattan, EcoHealth and its president, Peter Daszak, knew the virus was “capable of causing a worldwide pandemic.” Read more HERE.

Fauci successor at NIAID peddled dangerous Remdesivir drug as ‘silver bullet’ against covid: Dr. Jeanne Marrazzo tried to use unsafe antiviral intravenous drug on every covid hospitalised patient at University of Alabama at Birmingham. Prior to moving to her Government Health post, Marrazzo was the longtime director of the Division of Infectious Diseases at the University of Alabama at Birmingham (UAB). In partnership with Big Pharma drugmaker Gilead, UAB played a major role in the research and development of Remdesivir. Read more HERE.

Ruling on Remdesivir – manufacturer and hospital not protected by law: In a historic ruling, a judge in Michigan decided on 8 August that the Public Readiness and Emergency Preparedness (“PREP”) Act does not shield a drug manufacturer and a hospital in the case of a man who suffered two strokes and had to undergo a leg amputation due to receiving remdesivir, a covid-19 medication that was contaminated with glass particles. Read more HERE.

YouTube updates to its so-called “medical misinformation” policy: ”As you might imagine, the noose just got tighter on what YouTube believes to be “harmful” claims about covid, vaccines and cancer treatments. Harmful? Really? Let’s play that out for a moment.

One such “harmful claim” that was wiped from social media during the pandemic was that “ivermectin is effective for the prevention and treatment of every phase of covid-19 disease.” It was censored because ivermectin was getting in the way of achieving the successful roll-out of the vaccine. Read more HERE.