Wednesday, December 3, 2025

 

Certain bodybuilding and ayurvedic products put consumers at risk 

FDA is concerned about the potential health risks associated with products that claim to treat a variety of health issues or conditions. Consumers should avoid products marketed as supplements or other types of products that claim to have effects similar to prescription drugs.  

These products are a waste of money and there is no guarantee these fraudulent products will work as they claim they will. Many of these products pose a serious risk to your health and can have life-threatening outcomes. Bottom line: If it seems too good to be true, it probably is. 

Learn More

Tuesday, December 2, 2025

FDA Seizes 7-OH Opioids to Protect American Consumers; seizure focused on foods and dietary supplement products—including liquid shots and tablets—

 The U.S. Food and Drug Administration, in coordination with the U.S. Department of Justice, announced today that the U.S. Marshals Service seized approximately 73,000 units of 7-hydroxymitragynine (7-OH) products—valued at roughly $1 million—from three firms in Missouri.

The seizure focused on foods and dietary supplement products—including liquid shots and tablets—containing concentrated 7-OH as an added ingredient. Concentrated 7-OH is increasingly recognized as having potential for abuse because of its ability to bind to opioid receptors. It cannot be lawfully added to dietary supplements or conventional foods. These products are considered adulterated because 7-OH does not meet applicable safety standards. Also, the FDA has not approved 7-OH for medical use.

“This enforcement action is a strong step to protect Americans from the dangers of concentrated 7-OH products, which are potent opioids,” said FDA Commissioner Marty Makary, M.D., M.P.H. “We must be proactive and vigilant to address emerging threats to our communities and our kids.”

The FDA worked closely with the Missouri Department of Health and Senior Services in this enforcement action, which builds on the FDA’s comprehensive efforts to protect Americans from dangerous, illegal opioid substances. In July of this year, the FDA recommended the scheduling of certain 7-OH products under the Controlled Substances Act and issued warning letters to companies for illegally distributing products containing 7-OH, including tablets, gummies, drink mixes and shots. FDA also notified health care professionals and informed consumers of the risks associated with concentrated 7-OH products.

“The rise in the use of concentrated 7-OH as an illegal ingredient in foods and dietary supplements is of particular concern for the FDA,” said FDA Deputy Commissioner for Human Foods, Kyle Diamantas, J.D. “Actions like those announced today put a marker down that our agency will not tolerate the use of this dangerous ingredient in foods and dietary supplements, especially in products that are accessible to our nation’s youth.”

These recent operations demonstrate coordinated federal enforcement efforts against concentrated 7-OH products. The FDA reminds all manufacturers and distributors that they must ensure their products comply with all applicable federal requirements.

 


PBM Reforms: Are Sweeping Changes in Store for a Much-Maligned Industry?
On the surface, the chief factors behind the perennially escalating costs of prescription drugs consumed by Americans appear to be threefold: pharmaceutical companies, ...
Read More →

Wednesday, November 19, 2025

 

 

 

 

Friday, October 31, 2025

 

FDA Issues Emergency Use Authorization for New World Screwworm Drug for Dogs

The U.S. Food and Drug Administration today issued an Emergency Use Authorization (EUA) for Credelio (lotilaner) chewable tablets, concluding that, based on the scientific evidence available, it is reasonable to believe that Credelio may be effective in treating New World screwworm (NWS) infestations in dogs and puppies and the known and potential benefits of the product outweigh its known and potential risks. This is the first time ever that the FDA has issued an EUA for an animal drug.

“The FDA acted swiftly to make a screwworm treatment available for dogs in the U.S.,” said FDA Commissioner Marty Makary, M.D., M.P.H. “When it comes to emerging animal health threats, we need to be proactive, not reactive.”

“The FDA is using EUAs to bolster our nation’s preparedness for NWS,” said Timothy Schell, Ph.D., director of the FDA’s Center for Veterinary Medicine. “We are working expeditiously to review additional product-specific NWS EUA requests for animals that could be affected by NWS, including livestock, companion animals and wildlife.”

While the majority of dogs in America are at low risk of NWS due to their geographic location, dogs near the U.S.-Mexico border and dogs that have traveled to countries with active NWS cases are more likely to be exposed to NWS.

The risk to human health from NWS in the United States remains very low. Although eradicated from North America and Central America decades ago, NWS has progressed north since 2022. The parasite poses an emerging threat to livestock and food security, with potential impacts on both national security and animal health. NWS infests warm-blooded animals, including livestock, pets, wildlife, and, in rare cases, humans, causing severe tissue damage and sometimes death.

In August 2025, the Secretary of Health and Human Services determined that NWS presents a significant potential for a public health emergency and gave FDA the ability to issue EUAs for animal drugs to prevent or treat NWS. This EUA will be effective until it is revoked or the HHS Secretary terminates the declaration.

The FDA originally approved Credelio in 2018 for flea and tick-related indications in dogs and puppies.  

Lotilaner, the active ingredient in Credelio, belongs to a class of antiparasitic drugs called isoxazolines. Although isoxazoline products are commonly used and safe for most dogs, the products have been associated with neurologic adverse reactions, including muscle tremors, ataxia, and seizures. Pet owners should consult with a veterinarian to determine whether Credelio is appropriate for their pet.

Credelio is available only by prescription from a licensed veterinarian because professional expertise is required to monitor for and respond to potential adverse reactions. Detailed product information for veterinary practitioners can be found in the Fact Sheet for Veterinarians: Emergency Use Authorization of Credelio (lotilaner).