Legal Approaches to New Psychoactive Substances: First Empirical Findings

Jan van Amsterdam, Nicholas Burgess, Wim van den Brink

Research output: Contribution to journalReview articleAcademicpeer-review

Abstract

Background: Generic drug legislation, i.e., simultaneously banning groups of drugs, has been introduced worldwide to counteract the trade and use of emerging "new psychoactive substances"(NPSs) more effectively. Summary: The potential and de facto positive and negative effects of generic drug legislation have been described using an analysis based on documented evaluations of the experiences in the UK and Germany, supplemented with data from other publicly available sources. In particular, the effects of generic drug legislation on availability, use, sales, and overall health harms of NPS, and switches from NPS to traditional (classical) drugs are addressed. The results show that the introduction of generic drug legislation in the UK and Germany has enabled stricter regulation of NPS but has also led to some major harms within the domain of public health. Depending on the population considered, the rate of NPS use remained stable, slightly declined, or increased following the banning of NPS. Once banned, NPSs were more often purchased on the black market, often together with other (more harmful) drugs. Moreover, NPS-related harms did not reduce following the ban, and in some cases even increased. Finally, when harmful NPS, like potent synthetic opioids and cannabinoids, become substantially used and endanger public health, legislators already have the legal means to ban the problem drug, thus overruling the need for a generic ban.

Original languageEnglish
Pages (from-to)363-372
Number of pages10
JournalEuropean Addiction Research
Volume29
Issue number5
DOIs
Publication statusPublished - 1 Oct 2023

Keywords

  • Adverse effects
  • Generic drug legislation
  • Legislation
  • New psychoactive substances
  • Public health

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