The most commonly reported side effects of inotersen include platelet count decreased, protein urine present, and glomerular filtration rate decreased, based on 1,747 FDA adverse event reports from 2016 to 2025.
Percentages show how often each reaction appears relative to total reports for inotersen.
These are voluntary reports and do not establish that inotersen caused these reactions.
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Other drugs that appear in adverse event reports alongside inotersen. 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.
14.9% of inotersen adverse event reports involve female patients and 23.5% involve male patients. The largest age group is elderly at 61%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking inotersen when the adverse event was reported.
Showing 15 of 21 indications
Inotersen is sold under the brand name Tegsedi.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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