The most commonly reported side effects of tafamidis include death, off label use, and cardiac failure, based on 15,017 FDA adverse event reports from 2012 to 2025.
Percentages show how often each reaction appears relative to total reports for tafamidis.
These are voluntary reports and do not establish that tafamidis caused these reactions.
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Seriousness is determined by the reporter, not by OpenClaim.
Other drugs that appear in adverse event reports alongside tafamidis. 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.
17.3% of tafamidis adverse event reports involve female patients and 71.7% involve male patients. The largest age group is elderly at 95%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking tafamidis when the adverse event was reported.
Showing 15 of 257 indications
Tafamidis is sold under brand names including Vyndamax, Vyndaqel.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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