The most commonly reported side effects of cipaglucosidase include pneumonia, product dose omission issue, and fatigue, based on 60 FDA adverse event reports from 2023 to 2025.
Percentages show how often each reaction appears relative to total reports for cipaglucosidase.
These are voluntary reports and do not establish that cipaglucosidase caused these reactions.
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Other drugs that appear in adverse event reports alongside cipaglucosidase. 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 cipaglucosidase adverse event reports involve female patients and 36.7% involve male patients. The largest age group is adult at 69%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking cipaglucosidase when the adverse event was reported.
Cipaglucosidase is sold under the brand name Pombiliti.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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