The pharmacologic and clinical properties of Oxis (formoterol) Turbuhaler

Allergy. 1998;53(42 Suppl):14-9. doi: 10.1111/j.1398-9995.1998.tb04888.x.

Abstract

Oxis Turbuhaler has been approved for use in Europe at doses of 6, 12, or 24 micrograms once or twice daily. It has a rapid onset of action (within minutes) and demonstrates a maintained effect on airway function (an improvement of 20-30 l/min in PEF is seen 12 h after dosing), and it is well tolerated and safe. It decreases the incidence of acute asthma attacks, stimulates an immediate increase in PEF (in the order of 40-45 l/min), is effective when given in conjunction with anti-inflammatory medication, and has been shown to maintain a level of asthma control in all studies performed. Hence, Oxis Turbuhaler is a clinically relevant tool for use in patients receiving inhaled corticosteroids who require additional control of their asthma symptoms.

Publication types

  • Review

MeSH terms

  • Administration, Inhalation
  • Asthma / drug therapy
  • Bronchodilator Agents / administration & dosage
  • Bronchodilator Agents / adverse effects
  • Bronchodilator Agents / therapeutic use*
  • Clinical Trials as Topic
  • Dose-Response Relationship, Drug
  • Ethanolamines / administration & dosage*
  • Ethanolamines / adverse effects
  • Ethanolamines / therapeutic use*
  • Formoterol Fumarate
  • Humans

Substances

  • Bronchodilator Agents
  • Ethanolamines
  • Formoterol Fumarate