Dose-effect relationship of rilmenidine after chronic administration

Eur J Clin Pharmacol. 1993;45(2):157-60. doi: 10.1007/BF00315498.

Abstract

The antihypertensive efficacy and acceptability of 3 doses of rilmenidine (0.5, 1 and 2 mg, once daily) and a placebo over a 4 week period have been compared in a randomised, double-blind, parallel-group trial in 60 mild to moderate hypertensive patients. Six patients dropped out: 4 in the 2 mg-group and one in the 1 mg-group because of adverse events, and one in the placebo group for personal reason. The blood pressure was significantly decreased after the 1 and 2 mg doses with the maximum antihypertensive effect already being obtained after 1 mg. A significant dose-effect relationship was shown for supine systolic blood pressure (P = 0.05) but not for the supine diastolic blood pressure. The most beneficial efficacy/acceptability ratio was achieved at the dose of 1 mg once daily, which demonstrated the maximum antihypertensive effect associated with a low incidence of adverse events.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Antihypertensive Agents / administration & dosage*
  • Antihypertensive Agents / adverse effects
  • Antihypertensive Agents / therapeutic use
  • Blood Pressure / drug effects
  • Dose-Response Relationship, Drug
  • Double-Blind Method
  • Drug Administration Schedule
  • Female
  • Heart Rate / drug effects
  • Humans
  • Hypertension / drug therapy*
  • Male
  • Middle Aged
  • Oxazoles / administration & dosage*
  • Oxazoles / adverse effects
  • Oxazoles / therapeutic use
  • Rilmenidine
  • Supine Position

Substances

  • Antihypertensive Agents
  • Oxazoles
  • Rilmenidine