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1 ing responsiveness to inhaled salbutamol and ipratropium bromide.
3 ved either salmeterol 42 microg twice daily, ipratropium bromide 36 microg four times daily, or place
5 mpare the effects between pretreatments with ipratropium bromide and placebo aerosols on the airway r
7 butamol) and a short-acting anticholinergic (ipratropium bromide), in COPD is encouraging because the
11 sed it to study the effect of treatment with ipratropium bromide on the ability of the nose to condit
12 of a metered-dose inhaler containing either ipratropium bromide or placebo (two inhalations three ti
16 vere exacerbation of asthma, the addition of ipratropium bromide to albuterol and corticosteroid ther
20 ed (1:1) to receive nebulised salbutamol and ipratropium bromide with either 2.5 mL of isotonic MgSO(
21 atment group received 500 microg (2.5 ml) of ipratropium bromide with the second and third doses of a
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