The most commonly reported side effects of ipratropium include dyspnoea, asthma, and pneumonia, based on 79,107 FDA adverse event reports from 2004 to 2025. 6.0% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for ipratropium.
These are voluntary reports and do not establish that ipratropium caused these reactions.
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Other drugs that appear in adverse event reports alongside ipratropium. Drugs flagged as a suspected cause appear in the first column. Drugs taken at the same time but not suspected appear in the second.
Also suspected
Taken alongside
Co-occurrence in adverse event reports does not establish a drug interaction. Patients often take multiple medications, and these lists reflect prescribing patterns rather than causal relationships. Consult a healthcare provider about potential drug interactions.
55.5% of ipratropium adverse event reports involve female patients and 39.1% involve male patients. The largest age group is elderly at 54%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking ipratropium when the adverse event was reported.
Showing 15 of 746 indications
Ipratropium is sold under the brand name Combivent Respimat.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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