Alglucosidase Alfa

Category: Enzymes

Alglucosidase Alfa Overview

Alglucosidase 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).[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 Medical uses 2 Side effects 3 ...

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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.

Other drugs which contain Alglucosidase Alfa or a similar ingredient: (2 results)

LUMIZYME Alglucosidase Alfa
MYOZYME Alglucosidase Alfa