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The speaker discusses how CNN portrayed them as taking horse medication, specifically Ivermectin, which is actually a medication used more commonly in humans. They mention that Ivermectin has been prescribed to billions of people and even won a Nobel Prize for its efficacy in humans. The speaker believes that Ivermectin had to be discredited because of a federal law that states emergency use authorization for vaccines cannot be issued if there is an existing medication proven effective against the target illness. They argue that acknowledging the effectiveness of Ivermectin would have jeopardized the multi-billion dollar vaccine industry.

Ivermectin is a safe and effective drug for treating COVID-19, with studies showing it is safer than Tylenol and can help patients recover quickly, even those with low oxygen levels. A study in 2020 found a 50% reduction in hospitalizations when Ivermectin was used. Despite its proven benefits, hospital staff often resisted giving it to patients, leading to legal battles. However, when administered, even late in the illness, many patients improved and survived. The use of Ivermectin in hospitals is crucial for saving lives. Translation: Ivermectin es un medicamento seguro y efectivo para tratar el COVID-19, con estudios que muestran que es más seguro que el Tylenol y puede ayudar a los pacientes a recuperarse rápidamente, incluso aquellos con bajos niveles de oxígeno. Un estudio en 2020 encontró una reducción del 50% en hospitalizaciones cuando se usaba Ivermectin. A pesar de sus beneficios comprobados, el personal hospitalario a menudo se resistía a administrarlo a los pacientes, lo que llevaba a batallas legales. Sin embargo, cuando se administraba, incluso tarde en la enfermedad, muchos pacientes mejoraban y sobrevivían. El uso de Ivermectin en hospitales es crucial para salvar vidas.

The FDA now approves the use of Ivermectin for COVID treatment, which surprises the speaker. They discuss their previous conversations about finding alternative treatments for COVID and express frustration with the FDA's actions. They believe that many lives could have been saved if Ivermectin had been widely available. They mention the importance of truth and courageous reporting to counter the mainstream media's narrative. The speaker warns about the dangerous path the country is heading towards, with an elite group seeking control over people's lives. They highlight government expansion, WHO amendments, and the need for people to wake up to the current dangers.

Tony Fauci's problem is that a federal law prohibits emergency use authorization for a vaccine if there is an approved medication that is effective against the target disease. If Fauci had acknowledged the effectiveness of hydroxychloroquine or Ivermectin against COVID, it would have been illegal to approve the vaccines. The medical community, including 17,000 doctors, supported the use of these medications, but Fauci dismissed them as dangerous. It is speculated that Fauci had a strong incentive to discredit these medications. Many doctors, such as Harvey Reach, Peter McCulloch, and Pierre Corey, who have successfully treated COVID patients, believe that hundreds of thousands of American lives could have been saved if these medications were not suppressed.

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.

FDA attorney Ashley Chung Arnold acknowledges that doctors have the right to prescribe Ivermectin for COVID treatment. The FDA claims sovereign immunity and cannot be held responsible for misleading statements. The judges question whether the FDA's advice is based on scientific views or personal opinions. The FDA attorney argues that the agency is not required to go through a formal process and that they are accountable to the political process. The court is not responsible for fact-checking the FDA's scientific statements.

This year, it was revealed that $2.3 billion was allocated by the government, specifically the CDC and FDA, to pharmacies like Walgreens and CVS to discourage the prescription of ivermectin and other treatments recommended by doctors. The federal government has now acknowledged that these treatments were effective and expressed regret for suppressing them, admitting that this has led to unnecessary deaths. The influence of big pharma, particularly figures like Bill Gates, has resulted in restrictions on what healthcare professionals can prescribe, leading to consequences such as decertification and job loss for those who defy these guidelines. This situation highlights the dangers of a powerful cartel controlling medical practices.

I don't speculate on the motives of individuals like Anthony Fauci or Bill Gates; I focus on their actions. The narrative reveals serious immoral behavior linked to government positions. Recently, the FDA's chief attorney acknowledged there was no justification for discouraging the use of Ivermectin, which was an effective treatment for COVID. By withholding it and other existing remedies, millions died unnecessarily. The push for vaccines was prioritized, despite a federal rule preventing emergency use authorization if effective treatments were available. This led to a lack of proper testing for vaccines, resulting in alarming health issues, particularly myocarditis in young athletes. The rising number of athlete deaths on the field is unprecedented, and there remains a need for accountability as the science continues to emerge.

We found that the FDA lied about a maternal rat study that was testing the safety of mandating a vaccine to pregnant women. In every litter, individual pups had horrible bone deformities. This signal was extremely prominent. Moderna submitted the rat study, as they were required to do. The FDA then lied about the study results by claiming there were no problems. It was a huge enterprise in lying.

The FDA was sued over tweets telling people "you're not a horse" regarding Ivermectin. The lawsuit argued the FDA doesn't have the authority to tell people not to take a certain drug, as that constitutes practicing medicine. Some believe the FDA's actions were a coordinated PR attack to promote COVID vaccines. One doctor claims the government's agenda was to force vaccines, which are now known to be "poison jabs." The case against the FDA was settled largely on the plaintiffs' terms, with the FDA taking down the "offensive tweets." One doctor claims to have treated over 6,000 COVID patients with Ivermectin, with none hospitalized as a result, and considers it safer than common medications. The lawsuit set a precedent, potentially tarnishing the FDA's reputation and limiting future overreach in advising patients on medical treatments. Some believe the suppression of early COVID treatments has caused hundreds of thousands of deaths and that the COVID vaccines have caused excess deaths and increased disability.

Tony Fauci's problem is that a federal law prohibits emergency use authorization for a vaccine if there is an approved medication that effectively treats the target disease. If Fauci or anyone had acknowledged that Ivermectin works as a treatment for COVID, the vaccine would not have received authorization. Despite many doctors and publications supporting Ivermectin, Fauci actively dismissed it as a dangerous medication to drown out its effectiveness. It is unclear why he continued to do so after receiving authorization, but there is a strong incentive for him to discredit Ivermectin and hydroxychloroquine. Notable doctors like Harvey Reich and Pierre Cory have successfully treated thousands of COVID patients.

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.

Monoclonal antibodies worked very well and quickly, and were initially readily available. The speaker believes the government intentionally made them harder to get to encourage people to take the COVID shot. The speaker didn't use ivermectin until the government took over distribution of monoclonal antibodies. In March, the government put out information on why people should not take ivermectin for COVID on the FDA's website. At the same time, they launched COVID-nineteen Community Core on 04/01/2021, an $11,500,000,000 slush fund to feed out propaganda.

**Italiano:** Un'indagine biennale condotta da giornaliste mediche rivela che la FDA statunitense ha approvato centinaia di farmaci senza prove di efficacia, e talvolta nonostante prove di dannosità. Su oltre 400 approvazioni tra il 2013 e il 2022, il 73% non soddisfaceva i criteri fondamentali per l'efficacia, come gruppi di controllo e studi replicati. La FDA ha spesso optato per percorsi accelerati, ma molti studi di follow-up non vengono completati o non dimostrano l'efficacia. Più della metà delle approvazioni si basava su dati preliminari. In oncologia, solo 3 farmaci su 123 hanno soddisfatto tutti gli standard. Esempi includono Kopictra, che ha ridotto la sopravvivenza, e Elmiron, ancora in commercio nonostante la mancanza di efficacia e gravi effetti collaterali. Tra il 2018 e il 2021, sono stati spesi miliardi per farmaci con studi di follow-up incompleti. Si stima che 128.000 americani muoiano ogni anno a causa di farmaci prescritti correttamente. Molti medici non comprendono il processo di approvazione della FDA. Si evidenzia la dipendenza dell'agenzia dai finanziamenti dell'industria farmaceutica. **English Translation:** A two-year investigation by medical journalists reveals that the U.S. FDA has approved hundreds of drugs without proof of efficacy, and sometimes despite evidence of harm. Of over 400 approvals between 2013 and 2022, 73% did not meet fundamental efficacy criteria, such as control groups and replicated studies. The FDA has often opted for accelerated pathways, but many follow-up studies are not completed or do not demonstrate efficacy. More than half of approvals were based on preliminary data. In oncology, only 3 out of 123 drugs met all standards. Examples include Kopictra, which reduced survival, and Elmiron, still on the market despite lack of efficacy and serious side effects. Between 2018 and 2021, billions were spent on drugs with incomplete follow-up studies. An estimated 128,000 Americans die each year from correctly prescribed drugs. Many doctors do not understand the FDA approval process. The agency's dependence on pharmaceutical industry funding is highlighted.

Ivermectin is a widely used and safe drug that has been effective against SARS CoV 2. It could have saved many lives if it had been used more widely. Doctors who tried to use it faced prosecution, despite its safety and effectiveness. One doctor worked 715 continuous days without a day off because no one else wanted to care for indigent patients. The doctor's hospital had a low mortality rate compared to the rest of the country, thanks to protocols that included Ivermectin. However, the media ignored their success and the use of repurposed drugs. The doctor faced censorship on social media platforms for mentioning Ivermectin. The FDA claims there are no adequate alternatives to the vaccines, but many believe unnecessary deaths occurred due to censorship and lack of access to Ivermectin.

An experimental drug called remdesivir will be responsible for people's deaths. People diagnosed with COVID-19 in the hospital died between day one and day nine, specifically on day nine of a ten-day remdesivir treatment. Dr. Anthony Fauci claimed in May 2020 that remdesivir was found safe and effective in a drug trial in Africa a year earlier (02/2019), and hyperlinked the study in a memo to hospitals. However, in that trial, remdesivir killed 53% of people, and the safety board suspended its use at month six, deeming it too deadly and toxic for Ebola patients. Dr. Anthony Fauci and his department at the NIH funded the Ebola trial in Africa in 02/2019. Therefore, Fauci lied to Congress and the American people by claiming the drug was safe and effective against Ebola, when the safety board had deemed it too deadly and pulled it from the trial.

Speaker 0: I find information like this, you know, inserts for the vaccine. Paper's there, and there's nothing printed on it. I find that very interesting, disheartening, disgusting, and lots of other words, but then it gets better. It just keep wait. There's more. It just keeps happening. The CDC redacts every single word of a 148 page study on a myocarditis after COVID vaccination. So I asked research to print the study for me. 148 pages. The entire thing is redacted. What good does a study do if there's nothing there? Then I wanna know, wait, what might have been there that they needed to redact it? That's even scarier. Speaker 1: We're witnessing an active cover up of a colossal consumer product safety debacle that is is basically affecting the entire world. Mhmm. So in The United States, our CDC, National Institutes of Health, and the FDA are actively involved in a cover up. And the same is occurring in The UK with the MHRA, Europe with European medicine agencies, and Australia with the Therapeutic Goods Administration. Something is going on that's very big. Each one of these companies that puts out a product has an obligation to produce ninety days of safety monitoring after their product comes out. It's a regulatory dossier. If somebody has a problem with the new product and they call the company like Pfizer, Pfizer has to report, write down what happened, and they have to collate that in a report and produce it and make it publicly available. When it came to ninety days with Pfizer, the first vaccine that came out, remember Pfizer was approved 12/10/2020. Pfizer didn't produce the report. And then people started asking, well, what's happening with your vaccine? And Pfizer would not disclose what happened. And then it went to court. And the lawyer for the FDA stepped in and said they don't wanna release Pfizer's dossier for fifty five years. Mhmm. Oh. Fifty five years. And the the the plaintiff pushed. And finally, slowly, the Pfizer dossier came out. Pfizer recorded one thousand two hundred and twenty three deaths with their product within ninety days of release. People were calling Pfizer in desperation watching their family members die after taking the vaccine. Pfizer recorded over twelve hundred new adverse events, new problems that doctor Boden has talked to you about that we are grappling with the entire time. But the point is our FDA worked to cover this up. The FDA should be regulating this company. FDA should have been having at least monthly meetings and fully disclosing what was going on with these novel vaccines, which are a genetic transfer technology platform.

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.

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.

There is a growing problem of people using a drug meant for animals to treat COVID-19. This false information started with a viral video from a group called America's frontline doctors, claiming that hydroxychloroquine could cure COVID. They later started promoting another drug called Ivermectin as a cure for COVID, despite warnings from the CDC, FDA, and other health organizations that it is not effective and could be harmful. Ivermectin is actually meant to prevent parasites in animals like horses. It's important to rely on approved treatments and vaccines to prevent COVID-19.

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.

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.

According to a lawyer representing the FDA, doctors are now allowed to prescribe Ivermectin to treat COVID-19. This is a surprising development, as the FDA previously discouraged the use of Ivermectin for COVID-19. The case was brought by three doctors who claimed that the FDA unlawfully interfered with their medical practice by discouraging the use of Ivermectin. The FDA stated that Ivermectin is not authorized or approved to treat COVID-19. However, the doctors feel vindicated by this recent decision and are calling for accountability from the FDA. Stay tuned for more updates.

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.

The speaker believes that Ivermectin's effectiveness threatened the emergency use authorization for vaccines, which would impact the global market worth over $100 billion. The speaker suggests that Ivermectin's low cost and availability posed a threat to patented pharmaceuticals like PAXLOVID and Molnupiravir. They argue that Ivermectin could have ended the pandemic if widely used, but was suppressed due to its potential impact on the market. Translation: The speaker suggests that Ivermectin's effectiveness posed a threat to the emergency use authorization for vaccines and the global market, potentially impacting billions in revenue. They argue that Ivermectin's affordability and availability could have ended the pandemic if widely used, but was suppressed due to its potential impact on the market.