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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.

Paxlovid is a Pfizer drug for mild to moderate COVID-19 in those at high risk for progression to severe disease, including hospitalization or death. This is a combination medication that includes a repurposed HIV drug. There is a black box warning. "Paxlovid includes ritonavir, a strong CYP3A inhibitor." "Which may lead to greater exposure of certain concomitant medications resulting in potentially severe life threatening or fatal events." The package insert lists interactions with many meds, including statins, warfarin, SSRIs, birth control pills, and ED medications; the pharmacist should review the list before giving Paxlovid. The product is used under emergency use authorization; section 13.1. Carcinogenicity studies have not been conducted: "Dose dependent increase in the incident of adenomas, a type of tumor, and, and combined carcinomas in the liver." "So the bottom line is this." If you read through the package insert, this drug has all kinds of problems, which is why I don't use it. So great caution should be used before considering Paxlovid. Alternatives include ivermectin, hydroxychloroquine, nutraceuticals.

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.

Ivermectin is a versatile drug with antiviral and anti-inflammatory properties that stimulate healing processes like autophagy and improve the microbiome. It is effective for early COVID treatment and vaccine injuries, and is affordable as a generic drug. Despite misconceptions, it is not a horse dewormer and has been available for as little as 2¢ per tablet through the WHO.

200 congresspeople have been treated with Ivermectin for COVID, which was a common off-label treatment before vaccines were available. The motivation behind the negative perception of this medication is unclear, but it may relate to financial interests since Ivermectin is a generic drug with a low cost of about 30 cents per dose.

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.

The FDA only approves emergency use authorization if there are no other alternatives. Ivermectin's effectiveness could have impacted vaccine approval. Powerful interests oppose Ivermectin due to financial reasons. Drug companies profit greatly from vaccines. Ivermectin is cheap and widely available. Merck's stance on Ivermectin changed after its patent expired. Paid articles may not always provide accurate information.

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.

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.

Two hundred congresspeople have been treated with ivermectin for COVID. I did not know that. You could probably find it on doctor Pierre Corey’s Twitter page. Before there were vaccines, this was a common treatment, an off-label treatment for COVID. I do not know what the motivation for demonizing this particular medication is. Again, I’m not a doctor, and I’m not a scientist. But I would imagine some of it has to do with money. The reason being is that it is a generic drug now. They’ve the patent has run out. So anybody can make it, and it’s worth, like, 30¢ a dose.

The forest plot shows COVID medicines, with only expensive ones approved in the US. Cheaper options were ignored. Study endpoints were changed when results weren't as expected. Despite positive outcomes in trials, hydroxychloroquine and Ivermectin face negative perceptions in the US. Over 420 trials on hydroxychloroquine and 100 on Ivermectin show significant benefits, but they are still viewed negatively.

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.

Joe Rogan announced on social media that he has COVID and mentioned taking Ivermectin as part of his treatment. However, Ivermectin is primarily used as a dewormer for horses and is not proven to be effective against COVID. In fact, it can be dangerous and potentially deadly. The CDC and FDA have issued warnings against using Ivermectin for COVID. Some doctors claim that Ivermectin is effective and have faced backlash for advocating its use. There are allegations that pharmaceutical companies and the media have influenced the narrative against Ivermectin due to financial interests. Studies on Ivermectin have shown mixed results, but some countries have reported success in using it to treat COVID.

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.

Ivermectin, a drug discovered in the late seventies, has had a significant positive impact on billions of people worldwide. However, it has been wrongly portrayed as a horse poison. Despite being one of the safest drugs in history, Dr. Fauci claims it is dangerous. Similarly, hydroxychloroquine is dismissed as dangerous without proper evidence. Stephen Colbert, a propagandist, dismisses the effectiveness of these drugs without acknowledging their Nobel Prize-winning status and inclusion on the WHO list of essential medicines. This misinformation is fueled by their financial ties to Pfizer, leading them to deceive the public.

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.

Speaker claims ivermectin is part of a diabolical Rockefeller plan devised in 2010, predicting people would reject vaccines after 2020 and turn to another pharmaceutical. They question ivermectin’s safety by listing side effects such as blindness, liver failure, and infertility. They argue the Rockefellers own the entire medical system worldwide, so buying from a different country is ineffective. The discussion notes ads for pharmaceuticals on alternative-health platforms, suggesting a marketing push. They say parasites are really heavy metals in the body, and that ivermectin contains heavy metals. The claim is that ivermectin, like antibiotics, suppresses symptoms. They describe a $32,000,000,000 industry fueled by this narrative, and when they researched producers, they found Merck, Johnson and Johnson, Pfizer, and Bayer. The same companies making vaccines in 2020 allegedly also make ivermectin, framing it as a bait-and-switch.

The forest plot shows COVID medicines, with only expensive ones approved in the US. Cheaper drugs were ignored. Studies manipulated endpoints and faced negative PR. Over 420 trials on hydroxychloroquine and 100 on Ivermectin show significant benefits, but they are dismissed in the US.

200 congresspeople have reportedly been treated with Ivermectin for COVID, which was a common off-label treatment before vaccines were available. The motivation behind the negative perception of this medication is unclear, but it may be linked to financial interests. Ivermectin is a generic drug with a low cost of around 30 cents per dose, as its patent has expired, allowing anyone to produce it.

Pfizer knew their failed coronavirus modifications were dangerous, causing heart issues and death in animals. There is extensive literature, including patents and scientific publications, showing that they knew the heart was the target. The mRNA shots using pseudo uridine were known to generate tumors and rapid cancers. Remdesivir, with a 53% mortality rate, was chosen by the FDA as a COVID treatment, despite being deemed unethical by the World Health Organization due to its high death rate. The definition of adverse events was changed to exclude any causal link, allowing them to deny any negative effects. Data on these injections won't be published for another four and a half years.

Patients were desperate for ivermectin as their loved ones died, but the focus shifted to remdesivir, a previously failed Ebola drug. By November 2020, the World Health Organization advised against its use, citing ineffectiveness and potential kidney and liver damage. The European Society of Critical Care supported this stance. Despite the warnings, the U.S. Health and Human Services incentivized hospitals with a 20% bonus for administering remdesivir, leading to widespread use. It failed to reduce mortality and caused serious injuries, with some patients dying as a result. In May 2022, the WHO reaffirmed its initial decision, stating that remdesivir should never have been used.

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.