Did the New French Regulation of Zolpidem Decrease the Problematic Consumption of Zolpidem? A Field Study among Users

Int J Environ Res Public Health. 2022 Jul 22;19(15):8920. doi: 10.3390/ijerph19158920.

Abstract

Background: The French national drug regulatory authority stated, in 2017, that a secured prescription pad must be used for zolpidem prescriptions. This study aimed to evaluate the evolution of the problematic consumption of zolpidem at the individual level since the new regulation. Methods: Two nationwide populations of at-risk users of zolpidem were recruited: one in general practitioner (GP) offices and one in specialized care centers dedicated to drug dependence (SCDDs). Participants were asked about their zolpidem consumption before and after the regulation change. The primary outcome was the evolution of problematic zolpidem consumption, as defined by at least one of the following criteria: overconsumption, fraudulent ways of obtaining, effects sought other than hypnotic, and modes of administration other than oral. Results: A total of 243 participants were included: 125 from GP offices and 118 from SCDDs. In the GP population, the prevalence of patients who were identified as problematic consumers decreased from 24.8% to 20.8% (p = 0.593), whereas the prevalence decreased from 73.7% to 51.7% in the SCDD population (p < 0.001). The most prevalent criteria for problematic status were overconsumption and fraudulent ways. Conclusions: The new French regulation of zolpidem had different impacts among two different populations of at-risk zolpidem consumers.

Keywords: drug regulation; patient-related outcome; problematic consumption; substance use disorder; zolpidem.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Humans
  • Hypnotics and Sedatives* / therapeutic use
  • Prescriptions
  • Prevalence
  • Substance-Related Disorders* / epidemiology
  • Zolpidem

Substances

  • Hypnotics and Sedatives
  • Zolpidem

Grants and funding

This research was funded (grant number: AAP-2017-027) by the French National Agency for Medicines and Health Products Safety (Agence Nationale de Sécurité du médicament et des produits de santé, ANSM). The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.