The most commonly reported side effects of levomethadyl include torsade de pointes, electrocardiogram qt prolonged, and chest pain, based on 15 FDA adverse event reports from 2004 to 2020.
Percentages show how often each reaction appears relative to total reports for levomethadyl.
These are voluntary reports and do not establish that levomethadyl caused these reactions.
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Other drugs that appear in adverse event reports alongside levomethadyl. 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.
60.0% of levomethadyl adverse event reports involve female patients and 33.3% involve male patients. The largest age group is adult at 92%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking levomethadyl when the adverse event was reported.
Levomethadyl is sold under the brand name Orlaam.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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