Europeiska unionen - danska - EMA (European Medicines Agency)

sanofi b.v. - avalglucosidase alfa - glycogen opbevaring sygdom type ii - andre alimentary tract and metabolism produkter, - nexviadyme (avalglucosidase alfa) is indicated for long-term enzyme replacement therapy for the treatment of patients with pompe disease (acid α-glucosidase deficiency).

Europeiska unionen - franska - EMA (European Medicines Agency)

sanofi b.v. - avalglucosidase alfa - maladie de stockage de glycogène type ii - d'autres tractus digestif et le métabolisme des produits, - nexviadyme (avalglucosidase alfa) is indicated for long-term enzyme replacement therapy for the treatment of patients with pompe disease (acid α-glucosidase deficiency).

Europeiska unionen - tyska - EMA (European Medicines Agency)

sanofi b.v. - avalglucosidase alfa - glykogenspeicherkrankheit typ ii - anderen verdauungstrakt und stoffwechsel-produkte, - nexviadyme (avalglucosidase alfa) is indicated for long-term enzyme replacement therapy for the treatment of patients with pompe disease (acid α-glucosidase deficiency).

Europeiska unionen - nederländska - EMA (European Medicines Agency)

sanofi b.v. - avalglucosidase alfa - glycogeen opslag ziekte type ii - andere maagdarmkanaal en metabolisme producten, - nexviadyme (avalglucosidase alfa) is indicated for long-term enzyme replacement therapy for the treatment of patients with pompe disease (acid α-glucosidase deficiency).

Europeiska unionen - engelska - EMA (European Medicines Agency)

sanofi b.v. - avalglucosidase alfa - glycogen storage disease type ii - other alimentary tract and metabolism products, - nexviadyme (avalglucosidase alfa) is indicated for long-term enzyme replacement therapy for the treatment of patients with pompe disease (acid α-glucosidase deficiency).

Europeiska unionen - portugisiska - EMA (European Medicines Agency)

sanofi b.v. - avalglucosidase alfa - doença de armazenamento de glicogênio tipo ii - outro aparelho digestivo e metabolismo produtos, - nexviadyme (avalglucosidase alfa) is indicated for long-term enzyme replacement therapy for the treatment of patients with pompe disease (acid α-glucosidase deficiency).

Storbritannien - engelska - MHRA (Medicines & Healthcare Products Regulatory Agency)

special order - alglucosidase alfa - infusion - 1.6mg/1ml

Storbritannien - engelska - MHRA (Medicines & Healthcare Products Regulatory Agency)

special order - alglucosidase alfa - infusion - 1.9mg/1ml

Storbritannien - engelska - MHRA (Medicines & Healthcare Products Regulatory Agency)

special order - alglucosidase alfa - infusion - 2mg/1ml

Storbritannien - engelska - MHRA (Medicines & Healthcare Products Regulatory Agency)

special order - alglucosidase alfa - infusion - 2.2mg/1ml