Post marketing surveillance of zopiclone: interim analysis on the first 10,000 cases in a clinical study in general practice

Int Clin Psychopharmacol. 1990 Apr:5 Suppl 2:131-8.

Abstract

The tolerance of zopiclone, a hypnotic belonging to a new chemical group, the cyclopyrrolones, was studied in a follow-up trial in 23,000 insomniac outpatients treated for 3 weeks. The results from the interim analysis of the first 10,000 cases confirm the efficacy and safety of zopiclone under usual prescribing conditions. The average daily dose of zopiclone was 0.97 +/- 0.21 tablet (7.275 +/- 1.575 mg). The study population included 63.1% of female and 36.9% of male patients; the mean age was 52.3 +/- 16.6 years. 93.1% of the patients completed the trial. 8.2% of the patients experienced adverse reactions which resulted in drug discontinuation in only 2.8% of cases. In the global evaluation, the efficacy was rated excellent or good in more than 80% of the patients.

Publication types

  • Clinical Trial
  • Multicenter Study

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Arousal / drug effects
  • Azabicyclo Compounds
  • Family Practice
  • Female
  • France
  • Humans
  • Hypnotics and Sedatives*
  • Male
  • Middle Aged
  • Multicenter Studies as Topic
  • Piperazines / adverse effects
  • Piperazines / therapeutic use*
  • Product Surveillance, Postmarketing
  • Sleep Initiation and Maintenance Disorders / drug therapy*
  • Wakefulness / drug effects

Substances

  • Azabicyclo Compounds
  • Hypnotics and Sedatives
  • Piperazines
  • zopiclone