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AMA urges FDA to require clinical trials for botanical drug products

By Ella Ruder 1 min read

The American Medical Association is calling on the FDA to require botanical drug products, including kratom and cannabis, to prove safety and efficacy in clinical trials before they are marketed or prescribed, warning that unproven products can pose serious risks to patients. The AMA made its case in an Oct. 28 letter to FDA Deputy Commissioner Grace Graham. The physician group argued that rising consumer demand, anecdotal claims and influencer marketing on social media should not replace high-quality clinical trials or postmarket safety monitoring. AMA President Willie Underwood III, MD,… Originally published in Becker’s Hospital Review. Read More

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News Ella Ruder 4:30 pm National Council for Mental Wellbeing’s 4 priorities for Congress On Nov. 4, the National Council for Mental Wellbeing set four policy priorities for the 120th Congress and pledged to work with lawmakers from both parties to expand access to mental health and substance use care. The Washington, D.C.-based organization represents about 3,000 mental health… News Ella Ruder 12:38 pm Where 5 health systems are investing in interventional psychiatry For patients with treatment-resistant depression, the next step after medication and therapy is increasingly interventional psychiatry. Health systems are adding chairs for transcranial magnetic stimulation, moving to accelerated protocols that shrink weeks of treatment into days, and protecting electroconvulsive therapy programs even as rising costs… News Ella Ruder 11:54 am Illinois student mental health screenings face federal consent demand The U.S. Department of Education’s Student Privacy Policy Office demanded Oct. 30 that the Illinois State Board of Education revise its guidance on student mental health screenings, warning that conducting them without written parental consent and separating the results from education records could violate federal…

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