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Since May 2020, Remdesivir has been linked to a 30% death rate among patients receiving the drug for 5 to 10 days in hospitals. In New York, 26.9% of Medicare-aged patients who received Remdesivir died. The Cardiovascular Toxicology Journal found in October 2020 that Remdesivir is cardiotoxic and can cause death of heart cells. Despite this, the FDA and NIH continue to approve and recommend Remdesivir as the only drug for hospitalized COVID-19 patients. The World Health Organization published in April of last year that Remdesivir leads to increased acute kidney failure compared to other drugs. Shockingly, the FDA recently authorized the use of Remdesivir for newborns and children up to 18 years old.

I have a chart that shows the CDC and FDA's own numbers on adverse events. Despite social media censorship, these are the true numbers. Over 28 years of reporting, Ivermectin, Hydroxychloroquine, and Dexamethasone are shown to be safe drugs. However, since the COVID pandemic, remdesivir and the COVID vaccines have had adverse events. Our response to COVID has been a failure, with 4% of the world's population but supposedly 16% of the deaths. The VAERS system has recorded 1,600,000 adverse events from the COVID vaccines alone.

The FDA denies commanding against the use of Ivermectin for COVID as an off-label prescription, but acknowledges warning about potential risks. They sent a letter to medical boards and pharmacies stating that available data does not show Ivermectin's safety and effectiveness, mentioning side effects and potential dangers. The FDA's counsel mentioned that they also issue warnings for opioid drugs. Blue Cross, an insurance company, sent letters stating that Ivermectin should not be prescribed for COVID. The CDC, FDA, American Medical Association, and American Pharmacists Association have strongly warned against Ivermectin use. They mentioned insufficient data and potential fraud, waste, and abuse patterns. Doctors were warned that their prescribing behavior would be monitored, and inappropriate prescribing could lead to consequences and termination of participation.

We have a prevention protocol and an early treatment protocol. In the early treatment protocol, we use Ivermectin, which is not a horse dewormer. The claim that it's toxic is a complete lie. Over 3.7 billion doses of Ivermectin have been given to humans, making it one of the most influential drugs after penicillin. It is completely safe, even safer than Tylenol. While its efficacy can be debated, if you have limited options and a sick patient, why not try a safe and affordable drug like Ivermectin? There's nothing to lose.

Ivermectin is considered one of the safest medicines in history. It has a wide dosing range, making it difficult to overdose on. A comprehensive review by a French toxicologist found no documented deaths associated with Ivermectin, even with reports of massive overdoses. The World Health Organization (WHO) also acknowledges its safety, stating that most side effects are minor and temporary. In my experience, I have used Ivermectin for various diseases related to COVID, and the only potential side effects I have observed are occasional nausea, diarrhea, and blurry vision, which disappear once the medication is stopped. Overall, I cannot emphasize enough how safe and reliable Ivermectin is to use.

At home, it is recommended to treat viral replication by giving remedies like zinc and hydroxychloroquine, ivermectin, which reduce the spread of the disease. However, the protocol followed was different. No treatment was given until hospitalization, where ventilators and Remdesivir were used. It is known that Remdesivir can be harmful, as it caused side effects in Ebola patients. The drug was manipulated and made standard of care, leading to kidney failure, heart failure, and organ collapse in COVID-19 patients. The deaths during the pandemic were often attributed to kidney failure, which was caused by Remdesivir, not the virus itself.

Since May 2020, Remdesivir has been linked to a 30% death rate among patients receiving the drug in hospitals for 5 to 10 days. In New York, 26.9% of Medicare-aged patients who received Remdesivir died. The Cardiovascular Toxicology Journal found in October 2020 that Remdesivir causes heart cell death and is cardiotoxic. However, the FDA and NIH continue to approve and recommend Remdesivir as the only drug for hospitalized COVID-19 patients, despite the World Health Organization's report in April of last year that it causes increased acute kidney failure. Shockingly, the FDA recently authorized the use of Remdesivir for newborns and children up to 18 years old.

Since May 2020, remdesivir may result in at least 30% death in hospitalized patients who receive it for five to ten days. CMS data for Medicare patients in New York showed 26.9% of those who received remdesivir died. In October 2020, the cardiovascular toxicology journal found remdesivir causes death of heart cells, is cardiotoxic, and can lead to cardiac arrest. Despite this, in December 2020, the NIH, with Anthony Fauci, updated guidelines listing remdesivir as the only FDA-approved drug for hospitalized Americans, even though the WHO published data in April of last year that it increases acute kidney failure compared to other drugs used to treat COVID-19. As of January 21st of this year, the FDA extended emergency use authorization, making remdesivir the only authorized medication that can be administered intravenously to newborns to 18-year-olds for COVID-19.

Ivermectin is extremely safe, arguably safer than a sugar pill. In a randomized trial, those taking Ivermectin daily would likely experience fewer health issues than those on sugar pills. The narrative labeling Ivermectin as a toxic horse dewormer is misleading; over 3.7 billion doses have been administered to humans. It has significantly impacted global health by nearly eradicating several parasitic diseases. In fact, the risk of death from Tylenol is higher than from Ivermectin. While there are debates about its efficacy, in situations with limited options, using a safe and inexpensive drug like Ivermectin for sick patients seems reasonable.

When unable to use nirmatrlviriteonazia due to interaction issues, the REM des Ivir can be used instead. It is recommended to administer it in hospitals early on and ideally before the patient requires oxygen. This helps prevent the progression to severe forms of the condition.

In 2011, 2012, and 2014, publications revealed that pseudouridine in mRNA shots could cause rapid cancers. Remdesivir, with a 53% mortality rate, was chosen by the FDA for COVID treatment despite being deemed unethical by the World Health Organization due to high death rates in Africa. This lethal drug was administered regardless of viral load, resulting in unnecessary deaths.

In 2020, there was a disinformation campaign against Hydroxychloroquine, a generic drug. The pharmaceutical industry opposes generic drugs as they reduce profits. They conducted trials with toxic doses of Hydroxychloroquine, causing increased deaths. On the other hand, Ivermectin is beneficial when given in higher doses. The spike protein in COVID-19 causes clotting issues and suppresses interferon, a chemical that helps fight infections and cancer. Medicines like Ivermectin and others can boost interferon levels and prevent clotting by binding to receptors. Some patients given high doses of Ivermectin have shown remarkable recovery, as it competes with the spike protein for binding sites and prevents clot formation.

The speaker discusses the phenomenon of using drugs like ivermectin to treat COVID-19 without sufficient data to support its effectiveness. They emphasize the importance of safe and effective vaccines in preventing hospitalization and death from COVID-19. When patients request ivermectin, the speaker advises physicians to encourage vaccination for prevention and to provide monoclonal antibody treatment for those who qualify. For patients who are infected and at low risk for disease progression, the speaker suggests participating in clinical trials to determine the drug's efficacy. They provide the website clinicaltrials.gov for information on available trials.

Multiple studies, including one by the WHO, show that Remdesivir actually increases the risk of death. It's concerning that the federal government incentivizes hospitals to prescribe this toxic drug by offering a 20% bonus on the entire hospital bill for Medicare patients. Remdesivir costs around $3,000 per course. On the other hand, Ivermectin, as mentioned by Dr. Kory, reduces the risk of death by about 50%. Unfortunately, clinicians still use the wrong drug, Dexamethasone, in the wrong dose and for the wrong duration of time, simply because the NIH recommends it. The NIH and other agencies have disregarded multiple FDA-approved drugs that are both cost-effective and safe.

Ivermectin is safer than a sugar pill and has been given to billions of people with minimal harm. It is not a toxic horse dewormer, as claimed by the FDA. The drug is considered safe and has had a significant impact on global health by eradicating parasitic diseases. Despite debates on its effectiveness, it is a low-risk, affordable option for treating sick patients.

There are studies that suggest increased mortality with hydroxychloroquine, but there are also French studies that show a 50% decrease in deaths with its use. However, there is no significant difference in mortality rates. Some studies, including one from the CHU de Lyon, have shown serious side effects from hydroxychloroquine. Giving hydroxychloroquine to someone with a cardiac condition related to Covid increases the risk of cardiac complications. It not only lacks benefits but also increases the chances of intubation, ventilation, or death by 13%. Thankfully, the prescription of hydroxychloroquine in the community has been banned, which is considered a crucial public health measure that prevented potentially hundreds or even thousands of deaths.

To treat viral infections at home, zinc and its enhancers, like hydroxychloroquine and ivermectin, should be used, as they significantly reduce disease spread. However, the established protocol delayed treatment until hospitalization, where patients received ventilators and remdesivir—both potentially lethal. Remdesivir had previously shown harmful effects in Ebola trials, leading to its discontinuation due to a high rate of severe side effects. Despite this, it became standard care during the pandemic, contributing to kidney failure, heart failure, and organ collapse in patients. Many who died were reported to have kidney failure, which was not caused by the virus but rather by the effects of remdesivir.

Ivermectin is safer than a sugar pill, with minimal toxicity. It has been falsely labeled as a horse dewormer by the FDA, despite its extensive safe use in humans. Over 3.7 billion doses have been given, showing its safety. While its efficacy is debated, it is a low-risk, cost-effective option for treating sick patients.

The FDA's website advises against using ivermectin for COVID-19, yet links to clinical trials, half of which indicate it may be effective. For three years, the FDA has warned against ivermectin while referencing studies that support its use. Additionally, there is increasing research suggesting ivermectin could be a vital treatment for COVID-19. The strong opposition from the federal government appears to be linked to the desire to maintain emergency use authorization for COVID vaccines. For more insights, consider subscribing for additional videos.

Multiple studies show that of two, Moderna and Pfizer, Pfizer is definitely worse for cardiovascular side effects related to blood clotting, Pfizer is worse for neurologic effects, and Pfizer is worse for serious adverse events overall. A few studies have shown that Pfizer may be associated with be associated with an increase in mortality also compared to Moderna. The vaccines, they are not the same. Pfizer is definitely worse. You've got more myocarditis cases with Moderna, but Pfizer is worse overall. I apologize that it hasn't been clear. They shouldn't take them. They are products that should not be going into human Because these products, they should not used in any human beings. And, you know, there's some people who are trying to put them in animals too, and and I think many of us wouldn't wanna eat that food either, that meat. Along those lines, what's your recommendation?

Ivermectin, a Nobel Prize-winning anti-parasitic drug, has been vilified. Merck, who held the patent until 1996, claims it doesn't work for COVID-19. However, Merck has a 50/50 partnership with Moderna on mRNA cancer vaccines. Because Merck will make billions on mRNA cancer vaccines, they have no interest in investigating ivermectin for cancer. There is evidence that high-dose ivermectin is effective in treating many types of cancers.

PAXLOVID is claimed to be a potentially dangerous drug, more so than Ivermectin and hydroxychloroquine. It allegedly has 44 severe drug interactions, including with statins, and is supposedly toxic to the liver and kidneys. The drug purportedly contains an HIV drug with a black box warning. PAXLOVID is said to leave a bad metallic taste, leading to poor tolerance and early discontinuation, with a claimed 20% increase in rebound infections after stopping. The cash price is stated to be approximately $1200, leading to the assessment that it is a "trash drug."

Ivermectin is considered one of the safest medicines in history, with a wide dosing range and minimal side effects. A comprehensive review found no documented deaths associated with Ivermectin, even in cases of massive overdoses. The World Health Organization acknowledges that most side effects are minor and temporary, such as nausea, diarrhea, and blurry vision. As a physician, I find it to be a great medicine to work with due to its safety.

The FDA issues emergency use authorization for medical products when there are no approved alternatives. The effectiveness of Ivermectin as a treatment is questioned, as it would have affected the authorization of vaccines. Powerful forces with financial interests oppose Ivermectin, as it threatens global vaccination policies. Pharmaceutical companies like Pfizer, BioNTech, and Moderna have made significant profits from COVID-19 vaccines. Ivermectin is a cheap and widely available drug, but its safety is disputed by Merck, despite distributing it when it was under patent. It is important to be cautious of articles that may be biased or paid for.

I've stated since May 2020 that remdesivir will result in at least 30% death in those who receive it in the hospital. I had data pulled for Medicare patients in New York, and found that 26.9% of those who received remdesivir died. As of October 2020, the cardiovascular toxicology journal found that remdesivir causes death of heart cells and can lead to cardiac arrest. Yet, in December, the NIH decided to update all guidelines for treatment drugs allowed for COVID-19, and remdesivir was the only FDA-approved drug for hospitalized Americans, despite the WHO publishing that it causes increased acute kidney failure. As of January of this year, the FDA extended an emergency use authorization, making remdesivir the only authorized medication that can be administered to newborns to 18-year-olds.