Alglucosidase Alfa

Category: Enzymes



Alglucosidase Alfa Overview

Alglucosidase 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).[3] 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.[1] 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:

Alglucosidase Alfa
  • Injection: 20mg/kg
  • Powder: 5mg/ml
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

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