The FDA has settled a court case that alleged the agency overstepped with its campaign against ivermectin. The federal agency needs to remove every post or statement they made against ivermectin. This includes the most viewed post for the FDA on the platform X, in which they state, “You’re not a horse, stop it.”

The Front Line COVID-19 Critical Care Alliance (FLCCC) issued a press release regarding the settlement. Paul E Marik, M.D., was a plaintiff in the case and is the chairman and chief scientific officer of the FLCCC Alliance (FLCCC). He said, “The FDA interfered in the practice of medicine with their irresponsible language and posts about ivermectin. We will never know how many lives were affected because patients were denied access to a lifesaving treatment because their doctor was ‘just following the FDA.”

Ivermectin was highly publicized at the height of the pandemic as the number one podcast host in the world, Joe Rogan, said he took the medicine while he was sick with COVID-19. That prompted many mainstream media outlets to run stories stating that Joe Rogan took a horse dewormer drug instead of getting the vaccine. Rogan even threatened to sue CNN for their framing of the story because they failed to mention that ivermectin is also formulated for human use. 

The same thing occurred with the FDA’s famous “You’re not a horse” post. Despite this heavily shared post that lacks important context, the FDA has a page titled “Why You Should Not Use Ivermectin to Treat COVID-19“, which was last updated in December 2021, that provides this context. It says ivermectin is approved to treat “intestinal strongyloidiasis and onchocerciasis, two conditions caused by parasitic worms.”

This page also goes on to say that the FDA has not approved ivermectin for use in the treatment of COVID-19 and that there is no evidence it is safe or effective for this purpose. This page, which speaks primarily about ivermectin as a deworming drug for livestock, must be removed within 21 calendar days of the settlement, which falls on April 11, 2024. The settlement includes all other posts that indicate ivermectin should not be used to treat COVID–19 and posts on Twitter, LinkedIn, Facebook, and Instagram making similar references to ivermectin as a drug for horses. 

In the viral ivermectin post, the FDA presented an argument with logical fallacies. The red herring logical fallacy is when a misleading argument is presented to get the public to think in a certain way. The FDA did this when they said “You’re not a horse.” This is misleading because the drug is also formulated for humans and doesn’t address whether the medicine is suitable for COVID-19. 

In the FLCCC press release, Doctor Pierre Kory stated “The FDA knew exactly what it was doing when it tweeted that ivermectin was for horses and that people should ‘stop it.’ I hope this case will serve as precedent the next time a federal health agency steps out of its authority and tries to practice medicine.”

Dr. Kory is one of the doctors who researched the use of ivermectin and prescribed it to his patients in the treatment of COVID-19. He also authored the book The War On Ivermectin and made several appearances on The HighWire discussing the topic with Del Bigtree. A short film was published in December that can be viewed here

As Dr. Kory states, it is not the job of the FDA to practice medicine. It is fine for the FDA to state that a drug has not been approved for a specific use, but it is not within the realm of the agency to advocate against the off-label usage of a drug. 20% of all prescriptions made today are for off-label usage. It is not only legal for doctors to do so, but it is also common as it allows doctors to make the best choices for each individual patient. 

The three plaintiffs in the case were doctors who said the FDA campaign against ivermectin harmed their reputations. The three doctors are Robert L. ApterMary Talley Bowden, and Paul E. Marik. These doctors used their medical knowledge to prescribe the best treatments for their patients. The FDA tried to step in the middle of the doctor/patient relationship. These doctors endured censorship and harm to their reputations as a result. 

At the same time, the Murthy v. Missouri case continues as an important legal precedent for government-encouraged censorship of social media companies, which took place at the beginning of the COVID-19 pandemic. 

The FDA, CDC, and federal government provided strong messaging to encourage COVID-19 vaccine uptake and made declarations against alternative treatment options such as ivermectin. A viral post indicated that the FDA receives most of its funding from the corporations it regulates. The USA Today did a fact check to find that only 45% of the funding comes from application fees for when drug makers submit their product for approval. 

The amount of funds received by the FDA from the user fees increased by 42% between fiscal years 2017 and 2021. While USA Today rated the claim as mostly false, it upheld the truth that a large amount of funding to the FDA comes directly from the corporations they are regulating. Furthermore, a HighWire report from November went into more detail regarding the revolving door between the FDA and pharmaceutical companies, including Moderna. 

Regarding the outcome, Dr. Bowden stated, “This landmark case sets an important precedent in limiting FDA overreach into the doctor-patient relationship.”

Photo credit: https://twitter.com/mdbreathe/status/1771023714584273015?s=46&t=2tCbfuj36dolslMYQjC7Rg

 

 

Steven Middendorp

Steven Middendorp is an investigative journalist, musician, and teacher. He has been a freelance writer and journalist for over 20 years. More recently, he has focused on issues dealing with corruption and negligence in the judicial system. He is a homesteading hobby farmer who encourages people to grow their own food, eat locally, and care for the land that provides sustenance to the community.

Other Headlines

Coronavirus

CIA Whistleblower: “Dr. Fauci’s Role in the Cover Up Was Intentional”

CIA Whistleblower James E. Erdman III said “Dr. Fauci’s role in the (COVID-19) cover-up was intentional” during a Senate hearing Wednesday chaired by Senator Rand Paul. Erdman is a veteran with decades of experience in national security and intelligence, having served on the Director’s Initiatives Group (DIG) under DNI Tulsi Gabbard and worked for the CIAContinue reading CIA Whistleblower: “Dr. Fauci’s Role in the Cover Up Was Intentional”

More news about Coronavirus

Health & Nutrition

HHS Implements Strategy To Stop Overmedicalization With Psychiatric Medications

HHS is implementing a strategy and framework to reduce the overprescription of psychiatric medications. The administrators of four HHS agencies penned a Dear Colleague letter encouraging health care providers to provide full, informed consent for medications while prioritizing non-pharmacological methods as the first line of defense. “HHS encourages clinicians and provider organizations to support aContinue reading HHS Implements Strategy To Stop Overmedicalization With Psychiatric Medications

More news about Health & Nutrition

Vaccines

CIA Whistleblower: “Dr. Fauci’s Role in the Cover Up Was Intentional”

CIA Whistleblower James E. Erdman III said “Dr. Fauci’s role in the (COVID-19) cover-up was intentional” during a Senate hearing Wednesday chaired by Senator Rand Paul. Erdman is a veteran with decades of experience in national security and intelligence, having served on the Director’s Initiatives Group (DIG) under DNI Tulsi Gabbard and worked for the CIAContinue reading CIA Whistleblower: “Dr. Fauci’s Role in the Cover Up Was Intentional”

More news about Vaccines

Science & Tech

Anthropic Unauthorized Access Investigation Raises Questions About AI Safety Amidst Rapid Development

Anthropic is investigating a reported security breach that allowed a small group of people to gain access to Claude Mythos Preview, the company’s AI software that is too powerful to release to the public. AI models are becoming increasingly capable, and the 2026 International AI Safety Report notes that some hypothetical scenarios pose risks asContinue reading Anthropic Unauthorized Access Investigation Raises Questions About AI Safety Amidst Rapid Development

More news about Science & Tech

Environment

Supreme Court Considers Granting Bayer Protection From Pesticide ‘Failure-To-Warn’ Lawsuits

The U.S. Supreme Court heard oral arguments Monday about whether Bayer can be held liable for state-level failure to warn claims when the company followed EPA labeling guidelines after the federal agency classified glyphosate as “not likely carcinogenic to humans.” The court is not considering the underlying safety profile of glyphosate or Roundup, but theContinue reading Supreme Court Considers Granting Bayer Protection From Pesticide ‘Failure-To-Warn’ Lawsuits

More news about Environment

Policy

DNI Director Gabbard Investigates 120 US-Funded Biolabs For Gain-Of-Function Research

Director of National Intelligence Tulsi Gabbard is investigating over 120 biological laboratories outside of the country that were funded by US tax dollars as part of President Trump’s executive order to end dangerous gain-of-function research. Gabbard provided a statement to the New York Post on Monday saying her team will “identify where these labs are,Continue reading DNI Director Gabbard Investigates 120 US-Funded Biolabs For Gain-Of-Function Research

More news about Policy