Myozyme OverviewAlglucosidase alfa, sold under the brand name Myozyme among others, is an enzyme replacement therapy (ERT) orphan drug for treatment of Pompe disease (Glycogen storage disease type II), a rare lysosomal storage disorder (LSD). Chemically speaking, the drug is an analog of the enzyme that is deficient in patients affected by Pompe disease, alpha-glucosidase. It is the first drug available to treat this disease. It was approved for medical use in the United...
Read more Myozyme Details
Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Alglucosidase_alfa
Recent Myozyme Forums:Be the first to start a discussion about this drug.
Possible Dosages for this and Related Drugs:
- Injection: 20mg/kg
- Powder: 5mg/ml
NDC Database Records for Myozyme: (1 result)Sorted by National Drug Code
- 58468-0150 Myozyme 5 mg/ml Intravenous Injection, Powder, Lyophilized, for Solution by Genzyme Corporation