The most commonly reported side effects of avalglucosidase include drug specific antibody present, off label use, and weight increased, based on 827 FDA adverse event reports from 2012 to 2025.
Percentages show how often each reaction appears relative to total reports for avalglucosidase.
These are voluntary reports and do not establish that avalglucosidase caused these reactions.
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Other drugs that appear in adverse event reports alongside avalglucosidase. 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.
46.4% of avalglucosidase adverse event reports involve female patients and 40.5% involve male patients. The largest age group is adult at 62%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking avalglucosidase when the adverse event was reported.
Showing 15 of 19 indications
Avalglucosidase is sold under the brand name Nexviazyme.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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