The most commonly reported side effects of bitolterol include drug hypersensitivity, difficulty in walking, and hypersensitivity, based on 5 FDA adverse event reports from 2005 to 2020.
Percentages show how often each reaction appears relative to total reports for bitolterol.
These are voluntary reports and do not establish that bitolterol caused these reactions.
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Other drugs that appear in adverse event reports alongside bitolterol. 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.
80.0% of bitolterol adverse event reports involve female patients and 20.0% involve male patients. The largest age group is elderly at 80%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking bitolterol when the adverse event was reported.
Bitolterol is sold under the brand name Tornalate.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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