COVID-19 Drug Remdesivir Estimated to have Killed 100,000 Americans

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.”

FDA Approves Killer COVID Drug for Babies

While we have focused more on the COVID-19 vaccines that have created more deaths and injuries than all other FDA-approved vaccines for the previous 30 years, the other killer COVID drug currently being administered to the public is Remdesivir, with the brandname of “VEKLURY.” This drug, which was originally developed for ebola but never approved because it was so dangerous, has a history of scandals and many thousands of deaths since it was given an EUA (emergency use authorization) by the FDA, and then in October of 2020 it was fully approved by the FDA as a treatment for adults with COVID-19. To get the original EUA by the FDA, they had to attack existing drugs in the market that were already being proven as safe and effective against COVID-19 symptoms, such Ivermectin and hydroxychloroquine. A reasonable estimate of deaths caused by this killer drug worldwide would number in the millions. In September of 2021, Attorney Thomas Renz released to the public statistics on Remdesivir that a whistleblower had given to him from the CMS (Centers for Medicare & Medicaid Services) database, and the statistics were truly horrifying in terms of how many people were dying after taking this drug, which was over 25% of the patients. And now, the FDA has just approved this killer drug to be used with children, and babies as young as 28 days old.

FDA Shows Their Depth of Corruption by Approving Remdesivir for COVID with No Solid Proof the Drug Works

It was announced today that the FDA has now fully approved remdesivir (now called "VEKLURY" which already has a registered trademark, something that takes years to obtain generally) as a treatment for COVID. The path of getting remdesivir approved for use is one littered with corruption, and a process that has probably caused millions of deaths worldwide. (See our previous coverage.) One of the interesting side shows to watch during COVID is Big Pharma fighting each other as they compete for a bigger slice of the pie in COVID Government funding which is currently around 6-7 TRILLION dollars. We saw this earlier during the plandemic as many companies rushed to get COVID tests into the market. There are currently over 100 COVID tests that have been fast-tracked by the FDA, and these companies have attacked each other regarding the validity of their tests to the point where the CEO of one Big Pharma firm stated about one of his competitor's tests: “Not Worth Anything – Two of us could do it Overnight in the Garage.” So with remdesivir being the first COVID treatment receiving full approval by the FDA today, as opposed to merely "fast track" approval for emergency use, others in the Pharmaceutical Industry who are also rushing to get COVID drugs to market were quick to point out the lack of science backing up any evidence of effectiveness of remdesivir. Remdesivir, of course, was one of two experimental drugs that President Trump allegedly took that led to his "miraculous" cure from COVID, causing its stock to soar just when sales had slowed down.

Trump to do Full 5-Day Course of Remdesivir – Betrayal of Hydroxychloroquine Doctors?

Yesterday I speculated as to why President Trump may be receiving treatment for COVID as it was announced immediately after his alleged positive COVID test that he was going to be given a new experimental COVID drug that has not even been fast-tracked for approval yet. The stock of the company producing the drug rose on Friday as a result of the announcement. Today (October 4, 2020) it was announced that Trump had received his second dose of remdesivir, another experimental COVID drug, but one that has already received fast-track approval by the FDA, and has been widely distributed to hospitals. His doctors reported that President Trump would receive the full 5 doses. Interestingly, FiercePharma, the main pharmaceutical marketing trade publication, announced on Friday, October 2nd, the same day Trump was admitted to Walter Reed, that sales of Gilead's remdesivir were beginning to slump, and that the company was taking over distribution of the drug now as a result of the slow-down in sales. The cost for the 5-dose treatment of remdesivir is $3,120.00, and sales are expected to exceed $3.5 billion in revenue. Hydroxychloroquine (HCQ), a drug with no patents due to being in the marketplace with a perfect safety record for over 35 years and with a cost of about $20 per dose, was condemned by U.S. public health officials like Dr. Fauci as supposedly being ineffective in treating COVID. Gilead's remdesivir was given fast-track approval instead, and demand initially sky rocketed. But now, apparently the supply of remdesivir exceeds demand. That should change now that President Trump is using it, after initially taking HCQ as a preventive measure. As we have previously reported numerous times here at Health Impact News, Frontline Doctors and thousands of doctors around the world have successfully treated COVID patients with HCQ and many report a 100% success rate. I wonder how all of these doctors feel now, since most of them felt like President Trump was on their side since he had previously recommended HCQ? The demonization of HCQ in favor of Gilead's remdesivir has led to tens of thousands if not hundreds of thousands of unnecessary deaths, according to many doctors, making Dr. Fauci, FDA Commissioner Dr. Hahn, and others, complicit in mass murder. Are these Big Pharma mass murderers now forcing President Trump to promote their drugs to ensure his success in the elections?

Is the 100% Cure Rate of Hydroxychloroquine a Threat to Fast-Tracking the COVID Vaccines?

Medical journalist Del Bigtree of the weekly broadcast Highwire discussed on his show this week what he believes may be the primary reason why Fauci and the other political medical tyrants are so desperately trying to censor the positive results of Hydroxychloroquine (HCQ), a drug that has been around for over 65 years and is already FDA approved. The reason is probably because they want to force a COVID vaccine upon the public, and to do so, they need to fast-track the development of these vaccines, and then the FDA has to issue a an Emergency Use Authorization (EUA) to approve it. According to the "Qualifying Criteria" that allows the FDA to issue an EUA, there must be "No adequate, approved, and available alternative." HCQ is an "adequate, approved, and available" alternative, which should then disqualify any EUAs issued for a vaccine to treat COVID. The problem, of course, is that the Trump Administration has already given over $8 BILLION to Big Pharma to develop the vaccine in "Project Warp Speed," fast-tracking the vaccines development. In fact, this has already happened with Gilead's anti-viral drug Remdesivir, which was fast-tracked as a treatment for COVID and then issued an EUA. While the cost for the older HCQ medication is only about $20, Remdesivir's cost is about $3200.00. These mass murderers who call themselves "doctors" and claim absolute authority on medical issues do not treat patients themselves, but they control the FDA, the CDC, the NIH, and pretty much the entire Government. They don't value human life, and only want control so they can usher in their New World Order, and if a fast-tracked COVID vaccine ends up injuring and killing more people than COVID, it fits in perfectly with their plans for their New World Order and a One World Government as they seek to reduce the world's population of those they deem "non-essential."

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

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.