The most commonly reported side effects of aminohippurate include hypersensitivity, anaphylactic reaction, and infusion related reaction, based on 10 FDA adverse event reports from 2004 to 2023.
Percentages show how often each reaction appears relative to total reports for aminohippurate.
These are voluntary reports and do not establish that aminohippurate caused these reactions.
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Other drugs that appear in adverse event reports alongside aminohippurate. 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.
10.0% of aminohippurate adverse event reports involve female patients and 40.0% involve male patients. The largest age group is child at 75%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking aminohippurate when the adverse event was reported.
Aminohippurate is sold under the brand name Aminohippurate Sodium.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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