The most commonly reported side effects of t3) include weight increased, loss of consciousness, and insomnia, based on 135 FDA adverse event reports from 2004 to 2025. 6.7% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for t3).
These are voluntary reports and do not establish that t3) caused these reactions.
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Other drugs that appear in adverse event reports alongside t3). 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.
84.4% of t3) adverse event reports involve female patients and 11.1% involve male patients. The largest age group is adult at 58%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking t3) when the adverse event was reported.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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