Literature DB >> 45210

Oxitropium bromide (Ba 253), an advance in the field of anticholinergic bronchodilating treatments. Preliminary results.

A Minette, M Marcq.   

Abstract

The changes in FEV1 and in specific conductance induced by 200 micrograms oxitropium bromide given as pressurized aerosol were measured at 8 time intervals during 7 hours after inhalation in a group of 19 patients with reversible broncho-obstruction. The working of the drug was compared to the functional values observed at the same time intervals after placebo, 40 micrograms ipratropium bromide and 400 micrograms fenoterol. Both oxitropium and ipratropium were definitely and significantly superior to placebo at all time intervals. Oxitropium was superior to ipratropium at the 7th hour. At this time interval the difference was significant At the 7th hour oxitropium gave higher mean results than fenoterol, but this difference was not significant. The drug was also compared to its competitors regarding its subjective and cardiovascular tolerance. No unfavourable side-effects were observed.

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Year:  1979        PMID: 45210

Source DB:  PubMed          Journal:  Rev Inst Hyg Mines (Hasselt)        ISSN: 0301-3901


  4 in total

Review 1.  Long-acting beta2 agonists in the management of stable chronic obstructive pulmonary disease.

Authors:  M Cazzola; C F Donner
Journal:  Drugs       Date:  2000-08       Impact factor: 9.546

Review 2.  Anticholinergic agents for chronic asthma in adults.

Authors:  M Westby; M Benson; P Gibson
Journal:  Cochrane Database Syst Rev       Date:  2004

3.  Comparison of the bronchodilator activities of oxitropium bromide, fenoterol, and their combination in patients with chronic obstructive pulmonary disease and bronchial asthma.

Authors:  K Nishi; M Fujimura; S Myou; T Ooka; S Sakamoto; M Saitou; K Kasahara; T Matsuda
Journal:  Clin Auton Res       Date:  1993-02       Impact factor: 4.435

4.  Bronchodilator effects of oxitropium bromide, fenoterol, and their combination in normal subjects.

Authors:  M Fujimura; Y Kamio; T Matsuda; T Hashimoto
Journal:  Clin Auton Res       Date:  1993-02       Impact factor: 4.435

  4 in total

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