October 15, 2025

Suzanne Nielsen, João Pedro Silva, Jermaine D. Jones, Alex Krotulski, Dilkushi Poovendran, Deusdedit Muzangizi, Gilles Forte, Jason White, Sandra D. Comer

Drug and Alcohol Review

Abstract

Introduction
The global drug market has seen an emergence of potent synthetic opioids, including benzimidazole-derived substances known as nitazenes. These compounds have been implicated in fatal and non-fatal overdoses. This review aims to synthesise current evidence on the pharmacological effects, potency and naloxone responsiveness of new synthetic opioids, with a focus on synthetic opioids evaluated for international control since 2020. It highlights key findings that can inform our understanding of these substances and inform harm reduction strategies.

Methods
A narrative review was conducted using critical reviews from the World Health Organization Expert Committee on Drug Dependence and supplementary literature. Data extraction focused on pharmacological profiles, behavioural effects, potency estimates, and naloxone effectiveness.

Results
Thirteen synthetic opioids were examined, with potencies ranging from similar to morphine to exceeding that of fentanyl. Naloxone demonstrated efficacy in reversing overdose symptoms for most substances, although higher doses or infusions were occasionally required.

Discussion and Conclusions
The variability in nitazene potency and common unintended use underscores the need for widespread education, broad naloxone access and robust drug-checking initiatives. Key challenges include the detection of nitazenes in polydrug contexts and their presence in substances sold as other drugs, including falsified pharmaceuticals. Emerging evidence suggests that naloxone can reverse acute poisonings with benzimidazole opioids. However, no studies have examined the effectiveness of medications for treating opioid use disorder (e.g., methadone, buprenorphine, naltrexone) in people who are physically dependent on nitazenes. Future research should address this important knowledge gap.

FULL ARTICLE
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