Active Ingredient: Agalsidase alfa
Agalsidase alfa is indicated for long-term enzyme replacement therapy in patients with a confirmed diagnosis of Fabry Disease (α-galactosidase A deficiency).
For this indication, competent medicine agencies globally authorize below treatments:
Intravenous
0.2 - 0.2 mg per kg of body weight
From 0.2 To 0.2 mg per kg of body weight once every 14 day(s)
Agalsidase alfa is administered at a dose of 0.2 mg/kg body weight every other week by intravenous infusion over 40 minutes.
Intravenous infusion over 40 minutes.
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