The U.S. FDA and HHS have recommended reclassifying cannabis from Schedule I to Schedule III, citing its low abuse potential and low risk of physical and psychological dependence. The report was released following an F.O.I. request and sparked anticipation of DEA action for reclassification. However, it faces opposition from some congressional members citing an "irresponsible pro-cannabis agenda."
In August last year, the U.S. Department of Health and Human Services (HHS), along with the Food and Drug Administration (FDA), recommended reclassifying cannabis from Schedule I to Schedule III on the controlled substances list. However, the report had not been made public until now.
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The report’s publication follows a Freedom of Information Act request by lawyer Matt Zorn. The report is 252 pages long and highlights the FDA’s conclusions. According to Mr. Zorn’s analysis, the FDA identified three key criteria for reevaluating the list:
The FDA’s analysis compared the prevalence and harmful effects of cannabis to substances in Schedules I, II, and III. The agency found that the public health risks of cannabis are low compared to other drugs like heroin, cocaine, and benzodiazepines. The report emphasizes that “in terms of overdose deaths, cannabis consistently ranks at the bottom among comparison drugs.”
The FDA report confirms the credible medical use of cannabis in the treatment of anorexia, nausea, and pain. The agency assessed the potential benefits of cannabis for seven indications, including anxiety, epilepsy, inflammatory bowel diseases, and post-traumatic stress disorder. The conclusion highlighted strong evidence of cannabis’s effectiveness, particularly in treating anorexia related to medical conditions, nausea, and pain.
The publication of the FDA’s report has fueled expectations of imminent action by the U.S. Drug Enforcement Administration (DEA) to move cannabis from Schedule I to Schedule III in the U.S. President Joe Biden’s October 2022 directive, advocating for a swift review of cannabis classification, has accelerated the process. Legal experts anticipate a proposed regulation in the near future, with the final regulation expected by mid-summer.
While the FDA’s report has been hailed as a thorough and scientifically founded document, it faces opposition from some quarters. Republican members of Congress, citing an “irresponsible pro-cannabis agenda,” have expressed reservations about the FDA’s recommendation.
The DEA recently reiterated that it alone has the power to reclassify, or not, cannabis.
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(Featured image by Christa Dodoo via Unsplash)
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