The most commonly reported side effects of indigotindisulfonate include anaphylactic reaction, somnolence, and reaction to excipient, based on 5 FDA adverse event reports from 2008 to 2024. 20.0% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for indigotindisulfonate.
These are voluntary reports and do not establish that indigotindisulfonate caused these reactions.
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Other drugs that appear in adverse event reports alongside indigotindisulfonate. 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 indigotindisulfonate adverse event reports involve female patients and 40.0% involve male patients. The largest age group is elderly at 60%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking indigotindisulfonate when the adverse event was reported.
Indigotindisulfonate is sold under the brand name Bludigo.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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