The most commonly reported side effects of albumin iodinated i-125 serum include eye pain, headache, and off label use, based on 29 FDA adverse event reports from 2008 to 2025.
Percentages show how often each reaction appears relative to total reports for albumin iodinated i-125 serum.
These are voluntary reports and do not establish that albumin iodinated i-125 serum caused these reactions.
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Other drugs that appear in adverse event reports alongside albumin iodinated i-125 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.
48.3% of albumin iodinated i-125 serum adverse event reports involve female patients and 48.3% involve male patients. The largest age group is adult at 50%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking albumin iodinated i-125 serum when the adverse event was reported.
Albumin Iodinated I-125 Serum is sold under the brand name Jeanatope.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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