Citation

Weedn VW, Elizabeth Zaney M, McCord B, Lurie I, Baker A. J. Forensic Sci. 2021; ePub(ePub): ePub.

Copyright

(Copyright © 2021, American Society for Testing and Materials, Publisher John Wiley and Sons)

DOI

10.1111/1556-4029.14712

PMID

unavailable

Abstract

Fentanyl is now the primary driver of the current opioid crisis. Fentanyl and its analogues are subject to the Controlled Substances Act of 1970, the Controlled Substances Analogue Enforcement Act of 1986 (Federal Analogue Act), state laws, international treaties, and the laws of foreign countries. The appearance of novel psychoactive substances led to further legislative developments in scheduling. New fentanyl analogues proliferated in a manner previously unseen since about 2016. Overdose deaths of these fentanyl analogues prompted the Drug Enforcement Administration to reactively emergency schedule each new fentanyl analogue as it appeared. The international community also acted. Finally, on February 6, 2018, a proactive temporary (emergency) class-wide scheduling of fentanyl-related substances was implemented based upon the fentanyl core structure to save lives. This action spurred a similar action in China. Fentanyl analogues fell dramatically in the marketplace, despite further increases in fentanyl itself. Congress temporarily extended this scheduling, but it will soon expire. Opposition to permanent class-wide was lodged due to concerns over law enforcement overreach, inadequate Health and Human Services input, and hindrance of research. This paper reaffirms the importance of a class-based scheduling strategy while also arguing for increased research of schedule I controlled substances.

Language: en

Keywords

class-wide scheduling; Controlled Substances Act; fentanyl analogues; fentanyl-related substances; scheduling; temporary scheduling