Label Changes for:
Lumizyme (alglucosidase alfa)
July 2012
Changes have been made to the ADVERSE REACTIONS sections of the safety label.
Detailed View: Safety Labeling Changes Approved By FDA Center for Drug Evaluation and Research (CDER) – July 2012
ADVERSE REACTIONS
Postmarketing Experience
- abdominal pain, nephrotic syndrome and proteinuria, as observed events to the package insert

