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DEA orders probe of herbal medicine brand aeta

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The U.S. Drug Enforcement Administration is investigating the herbal product brand aetas, seeking information on its potential safety and efficacy.

The agency also is asking for additional samples to determine if any are contaminated with toxic chemicals, the Drug Enforcement Agency (DEA) said in a letter to a federal court. 

The DEA’s notice of intent to sue, dated Sept. 17, comes as Congress considers a bill that would ban herbal products containing ingredients with known or suspected toxicological effects. 

“This product is not authorized in the United States and has been withdrawn from the market,” DEA spokeswoman Emily McBride wrote in a statement to The Hill. 

As the DEA is seeking information about the product’s safety and effectiveness, it is asking to see “all records, tests, analyses, lab reports, and other records relating to the product, including all documents, documents, and materials related to the formulation, administration, use, packaging, and marketing of the product.”

Aetas is manufactured by San Diego-based Bioscience, which has offices in Colorado and Texas.

The company did not immediately respond to a request for comment.

The DEA has previously launched investigations into other herbal products, including the herb oatgrass and the herbal extract of sage.

A recent study found that the herb rosemary could cause “severe” adverse effects on liver, kidney, and brain function, according to a study published in the journal Toxicology and Applied Pharmacology.

“It’s not an FDA-approved product, but we have received reports of serious health impacts from some of the products on the market today,” Michael Vittorio, chief of the FDA’s Center for Drug Evaluation and Research, told The Hill in August.

“There are other herbs that have been in use for thousands of years, and there are other herbal supplements that are being studied by other scientists and regulators around the world.

I think we need to look at these more carefully.”

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