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Fentanyl‐related substance scheduling as an effective drug control strategy
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....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8360110/ https://www.ncbi.nlm.nih.gov/pubmed/33951192 http://dx.doi.org/10.1111/1556-4029.14712 |
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author | Weedn, Victor W. Elizabeth Zaney, Mary McCord, Bruce Lurie, Ira Baker, Andrew |
author_facet | Weedn, Victor W. Elizabeth Zaney, Mary McCord, Bruce Lurie, Ira Baker, Andrew |
author_sort | Weedn, Victor W. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8360110 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83601102021-08-17 Fentanyl‐related substance scheduling as an effective drug control strategy Weedn, Victor W. Elizabeth Zaney, Mary McCord, Bruce Lurie, Ira Baker, Andrew J Forensic Sci Commentary 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. John Wiley and Sons Inc. 2021-05-05 2021-07 /pmc/articles/PMC8360110/ /pubmed/33951192 http://dx.doi.org/10.1111/1556-4029.14712 Text en © 2021 The Authors. Journal of Forensic Sciences published by Wiley Periodicals LLC on behalf of American Academy of Forensic Sciences https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Commentary Weedn, Victor W. Elizabeth Zaney, Mary McCord, Bruce Lurie, Ira Baker, Andrew Fentanyl‐related substance scheduling as an effective drug control strategy |
title | Fentanyl‐related substance scheduling as an effective drug control strategy |
title_full | Fentanyl‐related substance scheduling as an effective drug control strategy |
title_fullStr | Fentanyl‐related substance scheduling as an effective drug control strategy |
title_full_unstemmed | Fentanyl‐related substance scheduling as an effective drug control strategy |
title_short | Fentanyl‐related substance scheduling as an effective drug control strategy |
title_sort | fentanyl‐related substance scheduling as an effective drug control strategy |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8360110/ https://www.ncbi.nlm.nih.gov/pubmed/33951192 http://dx.doi.org/10.1111/1556-4029.14712 |
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