• Alglucosidase alfa - Wikipedia, the free encyclopedia

    en.wikipedia.org/wiki/Alglucosidase_alfa Alglucosidase alfa (Lumizyme, Myozyme, Genzyme) is an enzyme replacement therapy (ERT) orphan drug for treatment of Pompe disease (Glycogen storage disease type II ...
  • Myozyme | Treatment for Pompe Disease

    www.myozyme.com The First Specific Treatment for Pompe Disease Myozyme ® (alglucosidase alfa) is a lysosomal glycogen-specific enzyme indicated for use in patients with Pompe ...
  • Alglucosidase alfa - Drugs.com

    www.drugs.com/cdi/alglucosidase-alfa.html Easy to read patient leaflet for alglucosidase alfa. Includes indications, proper use, special instructions, precautions, and possible side effects.
    • Alglucosidase alfa - Food and Drug Administration

      www.fda.gov/AboutFDA/CentersOffices/.../ucm221285.htm On May 24th, 2010, FDA approved alglucosidase alfa (Lumizyme). Lumizyme is indicated for patients 8 years and older with late (non-infantile) onset Pompe disease who ...
    • alglucosidase alfa (injection) | Cigna

      www.cigna.com/healthwellness/hw/medications/alglucosidase-alfa-d05787a1 Alglucosidase alfa contains an enzyme that naturally occurs in the body in healthy people. Some people lack this enzyme because of a genetic disorder. Alglucosidase ...
    • Alglucosidase Alfa - Side Effects, Dosage, Interactions ...

      www.everydayhealth.com/drugs/alglucosidase-alfa Alglucosidase alfa contains an enzyme that naturally occurs in the body in healthy people. Some people lack this enzyme because of a genetic disorder.