Efficacy and duration of action of oral procaterol in asthmatic children after single administration of different dosages

J Asthma. 1990;27(1):21-30. doi: 10.3109/02770909009073290.

Abstract

A double-blind crossover study was performed to evaluate the bronchodilating effect of different single doses of procaterol (less than 0.5 micrograms/kg, 1.5 micrograms/kg, and placebo) orally administered. Sixteen asthmatic children, age 6-12 years, participated in the trial. Pulmonary function, heart rate, blood pressure, and tremor were evaluated at 30, 60, 90, and 120 min and then hourly for 8 hours after administration. All three doses were therapeutically effective. The 1.5 micrograms/kg dose produced a more sustained bronchodilatation effect, but was also associated with an increase in the incidence of tremors. The 0.5 micrograms/kg dosage may, however, be a good starting dose because it assures a reasonable risk/benefit ratio.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial

MeSH terms

  • Administration, Oral
  • Asthma / drug therapy*
  • Asthma / physiopathology
  • Bronchodilator Agents
  • Child
  • Dose-Response Relationship, Drug
  • Drug Administration Schedule
  • Ethanolamines / administration & dosage*
  • Ethanolamines / adverse effects
  • Ethanolamines / therapeutic use
  • Forced Expiratory Volume / drug effects
  • Heart Rate / drug effects
  • Humans
  • Maximal Midexpiratory Flow Rate / drug effects
  • Procaterol
  • Time Factors
  • Tremor / chemically induced
  • Vital Capacity / drug effects

Substances

  • Bronchodilator Agents
  • Ethanolamines
  • Procaterol