The most commonly reported side effects of levobetaxolol include completed suicide, pruritus generalised, and rash generalised, based on 10 FDA adverse event reports from 2005 to 2025. 10.0% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for levobetaxolol.
These are voluntary reports and do not establish that levobetaxolol caused these reactions.
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Other drugs that appear in adverse event reports alongside levobetaxolol. 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.
40.0% of levobetaxolol adverse event reports involve female patients and 60.0% involve male patients. The largest age group is elderly at 63%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking levobetaxolol when the adverse event was reported.
Levobetaxolol is sold under the brand name Betaxon.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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