The most commonly reported side effects of albumin iodinated i-131 serum include dacryostenosis acquired, convulsion, and thrombocytopenia, based on 13 FDA adverse event reports from 2004 to 2025.
Percentages show how often each reaction appears relative to total reports for albumin iodinated i-131 serum.
These are voluntary reports and do not establish that albumin iodinated i-131 serum caused these reactions.
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Other drugs that appear in adverse event reports alongside albumin iodinated i-131 serum. 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.
38.5% of albumin iodinated i-131 serum adverse event reports involve female patients and 61.5% involve male patients. The largest age group is adult at 63%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking albumin iodinated i-131 serum when the adverse event was reported.
Albumin Iodinated I-131 Serum is sold under the brand name Megatope.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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