The most commonly reported side effects of pegzilarginase include vomiting, hyperammonaemia, and lethargy, based on 2 FDA adverse event reports from 2016 to 2025.
Percentages show how often each reaction appears relative to total reports for pegzilarginase.
These are voluntary reports and do not establish that pegzilarginase caused these reactions.
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Other drugs that appear in adverse event reports alongside pegzilarginase. 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.
50.0% of pegzilarginase adverse event reports involve female patients and 50.0% involve male patients. The largest age group is child at 50%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking pegzilarginase when the adverse event was reported.
Pegzilarginase is sold under the brand name Loargys.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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