Myozyme OverviewAlglucosidase alfa (Lumizyme, Myozyme, Genzyme) 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. Contents 1 Status 2 Side effects 3 References 4 External link...
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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
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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