The most commonly reported side effects of pentetate include fatigue, chest pain, and therapy cessation, based on 45 FDA adverse event reports from 2004 to 2025.
Percentages show how often each reaction appears relative to total reports for pentetate.
These are voluntary reports and do not establish that pentetate caused these reactions.
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Other drugs that appear in adverse event reports alongside pentetate. 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.
71.1% of pentetate adverse event reports involve female patients and 24.4% 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 pentetate when the adverse event was reported.
Pentetate is sold under brand names including Ytterbium Yb 169 Dtpa, Pentetate Zinc Trisodium, Pentetate Calcium Trisodium.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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