Abstract

PurposeDesigner benzodiazepines (DBZDs) increasingly emerged on the novel psychoactive substance (NPS) market in the last few years. They are usually sold as readily available alternatives to prescription benzodiazepines (BZDs) or added to counterfeit medicines. BZDs are generally considered relatively safe drugs due to the low risk of serious acute adverse effects in mono-intoxication, though e.g., alprazolam seems to display an elevated risk of respiratory depression. Here we report on a fatal intoxication involving the novel DBZD flualprazolam.MethodsA complete postmortem examination was performed. General unknown screenings and analysis of drugs of abuse were performed on postmortem samples by immunoassay, gas chromatography–mass spectrometry and liquid chromatography–mass spectrometry. The standard addition method was employed to quantify flualprazolam in postmortem blood and tissues. Finally, a toxicological significance score (TSS) was assigned.ResultsFlualprazolam was detected in heart serum (25.4 ng/mL) and peripheral blood (21.9 ng/mL) as well as in urine, stomach contents, brain, liver and kidney (65.2–323 ng/g). The cause of death was deemed as central nervous system (CNS) and respiratory depression with agonal aspiration of stomach contents, in the setting of a multiple drug intake. Given the concentration levels of the co-consumed CNS depressants, the contribution of flualprazolam to the death was considered likely (TSS of 3).ConclusionsOur results support that highly potent DBZDs like flualprazolam carry an elevated risk for unintended toxicity, especially in association with other CNS depressants. A multidisciplinary evaluation of fatalities remains mandatory, especially when pharmacological/toxicological data on intoxicating compounds are lacking. To our knowledge this is the first report of flualprazolam concentrations in solid tissues in human.

Highlights

  • The term ‘designer benzodiazepines’ (DBZDs) or ‘novel benzodiazepines’ usually refers to a class of new psychoactive substances (NPS) designed as alternative to ‘prescription-only’ or controlled benzodiazepines (BZDs)

  • The deceased was overweight and with shaved head

  • The heart showed a mild dilatation of the right chambers, atherosclerosis, with a noncritical stenosis (> 50%) at the left descending coronary artery, and patency of the foramen ovale

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Summary

Introduction

The term ‘designer benzodiazepines’ (DBZDs) or ‘novel benzodiazepines’ usually refers to a class of new psychoactive substances (NPS) designed as alternative to ‘prescription-only’ or controlled benzodiazepines (BZDs). The European Monitoring Centre for Drugs and Drug Addiction (EMCDDA) is monitoring 30 DBZDs, 21 of which have been offered on the NPS market only since 2015 [1]. Within the STRIDA project which monitors the occurrence of NPS related intoxications in Sweden, an increased rate of positive urine sample for DBZDs has been reported (from 4% in 2012 to 19% in 2015) [4]. In contrast to other central nervous system (CNS) depressants like barbiturates, BZDs are known to be relatively safe drugs. They are rarely found as the cause of death in mono-intoxications, the combination with other drugs and medications, e.g., opioids or alcohol, can lead to death [5,6,7]

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