FDA and ivermectin











>> YOUR LINK HERE: ___ http://youtube.com/watch?v=fR4jEvuoF6I

FDA explicitly recognizes that doctors do have the authority to prescribe ivermectin to treat COVID • Department of Justice lawyer representing the FDA • Circuit Judge Jennifer Walker Elrod • Ashley Cheung Honold • During oral arguments on Aug. 8, 2023 in the U.S. Court of Appeals for the 5th Circuit. • https://covid19.onedaymd.com/2023/08/... • • “FDA is clearly acknowledging that doctors have the authority to prescribe human ivermectin to treat COVID. • So they are not interfering with the authority of doctors to prescribe drugs or to practice medicine,” • Three doctors • Lawsuit filed by Boyden Gray Associates on behalf of three doctors who were disciplined for prescribing human-grade ivermectin to patients. • https://storage.courtlistener.com/rec... • FDA had violated well-established law that allows doctors to prescribe an FDA-approved drug as an off-label treatment. • FDA has unlawfully taken formal, unequivocal, and conclusory actions to prohibit or otherwise interfere with the use of ivermectin to treat COVID-19, • The FDA cannot advise whether or for what purpose a doctor should prescribe, or a patient should take, an approved drug, • Ivermectin approved by FDA in 1966 • Case rejected late 2022 • Not surprising its horse medicine • https://www.fda.gov/consumers/consume... •   / 1429050070243192839   • At the appeal • What about when it said, ‘No, stop it’?” • (Circuit Judge Jennifer Walker Elrod) • “Why isn’t that a command? If you were in English class, they would say that was a command.” • Ms. Honold described the statements as “merely quips.” • Is it horse and cow medicine? • https://www.ncbi.nlm.nih.gov/pmc/arti... • ‘more than 2.5 billion human (2,500,000,000) doses distributed in the last 30 years’ • On the WHO list of essential medicines • https://www.who.int/publications/i/it... • Emergency Use Authorization of Medical Products and Related Authorities • https://www.fda.gov/regulatory-inform... • d. No Alternatives • For FDA to issue an EUA, there must be no adequate, approved, and available alternative to the candidate product for diagnosing, preventing, or treating the disease or condition. • A potential alternative product may be considered “unavailable” if there are insufficient supplies of the approved alternative to fully meet the emergency need. • https://support.google.com/youtube/an... • Treatment misinformation: • We do not allow content that promotes information that contradicts health authority guidance on treatments for specific health conditions, • including promotion of specific harmful substances or practices that have not been approved by local health authorities or the World Health Organization as safe or effective, • or that have been confirmed to cause severe harm. • https://beckernews.com/now-that-the-c... • https://www.theepochtimes.com/health/... • https://www.ncbi.nlm.nih.gov/pmc/arti... • https://www.ncbi.nlm.nih.gov/pmc/arti...

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