The most commonly reported side effects of velaglucerase include inappropriate schedule of product administration, product dose omission issue, and covid-19, based on 1,980 FDA adverse event reports from 2010 to 2025.
Percentages show how often each reaction appears relative to total reports for velaglucerase.
These are voluntary reports and do not establish that velaglucerase caused these reactions.
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Other drugs that appear in adverse event reports alongside velaglucerase. 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.
49.3% of velaglucerase adverse event reports involve female patients and 39.8% involve male patients. The largest age group is adult at 54%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking velaglucerase when the adverse event was reported.
Showing 15 of 53 indications
Velaglucerase is sold under the brand name Vpriv.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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