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As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work.Articles
From Schedule I to the Clinic—Insights Into Psychedelic Drug Development From GHB
Tiffany Farchione, MD, Director of the US Food and Drug Administration’s (FDA) Division of Psychiatry, recently told an audience that “Fully a third of my workload at this point [is] just reviewing psychedelic [investigational new drug applications].”1 The breadth and pace of today’s pharmaceutical development of these Schedule I substances may be unprecedented, yet a Schedule I substance securing FDA approval is not.
Strengthening Safeguards for Psychiatric Uses of Ketamine
Strengthening Safeguards for Psychiatric Uses of Ketamine In recent years, off-label use of ketamine has surged in the US. Data from more than 125 million patients indicate that ketamine prescriptions grew from 0.55 per 100 000 people in 2017 to 3.01 per 100 000 people in 2022—a 5.5-fold increase.1 The proportion of patients prescribed ketamine with billing diagnoses of depression increased from 5.3% to 28.3% during that period.1
Eliminating the Medicare Coverage Gap for Intranasal Naloxone and Nicotine Replacement Therapy
Eliminating the Medicare Coverage Gap for Intranasal Naloxone and Nicotine Replacement Therapy Opioid and tobacco use disorders are leading causes of preventable deaths in the US.
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