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Home > Report on the risk assessment of N-(1‑phenethylpiperidin-4-yl)-N-phenylacrylamide (acryloylfentanyl) in the framework of the Council Decision on new psychoactive substances.

European Monitoring Centre for Drugs and Drug Addiction. [EMCDDA] (2017) Report on the risk assessment of N-(1‑phenethylpiperidin-4-yl)-N-phenylacrylamide (acryloylfentanyl) in the framework of the Council Decision on new psychoactive substances. Luxembourg: Publications Office of the European Union. 50 p.

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EMCDDA Risk Assessments are publications examining the health and social risks of individual new psychoactive substances.

This publication presents the data and findings of the risk assessment on N-(1‑phenethylpiperidin-4-yl)-N-phenylacrylamide (acryloylfentanyl), carried out by the extended Scientific Committee of the EMCDDA on 22 February 2017. On the basis of the Risk Assessment Report — and on the initiative of the European Commission — on 25 September 2017, the Council decided that acryloylfentanyl should be subject to control measures across the Member States.

Acryloylfentanyl is known from the scientific literature and is a close structural relative of fentanyl. Fentanyl is a fast but short-acting synthetic opioid.

Table of contents:
• EMCDDA actions on monitoring and responding to new drugs
• EMCDDA–Europol Joint Report on acryloylfentanyl: a summary
• Risk Assessment Report of a new psychoactive substance: acryloylfentanyl
• Annex 1: Technical report on acryloylfentanyl
• Council Decision on subjecting acryloylfentanyl to control measures
• Participants of the risk assessment meeting


Item Type
Evidence resource
Publication Type
Guideline
Drug Type
Opioid, New psychoactive substance
Intervention Type
AOD disorder harm reduction
Source
Date
5 December 2017
Pages
50 p.
Publisher
Publications Office of the European Union
Corporate Creators
European Monitoring Centre for Drugs and Drug Addiction
Place of Publication
Luxembourg
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