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Drug Name:


Generic Name and Formulations:
Agalsidase beta 5mg, 35mg; per vial; lyophilized pwd for IV infusion after reconstitution and dilution; preservative-free.

Sanofi Genzyme Company

Therapeutic Use:

Indications for FABRAZYME:

Fabry disease.

Adults and Children:

<8yrs: not established. Pretreat with antipyretic and antihistamine. Give by IV infusion. ≥8yrs: 1mg/kg every 2 weeks. Initially infuse at a rate of ≤0.25mg/min; if tolerated, may increase by increments of 0.05–0.08mg/min with each subsequent infusion. <30kg: max rate 0.25mg/min. ≥30kg: minimum duration is 1.5hrs. Slow rate if infusion reactions occur. Rechallenge: initially give a low dose and infusion rate (eg, 0.5mg/kg at 0.01mg/min); once tolerated, may increase dose to 1mg/kg, titrate rate slowly upwards (doubled every 30mins up to max 0.25mg/min); see full labeling.


Have appropriate medical support measures readily available; discontinue if anaphylaxis or severe allergic reactions occur. Compromised cardiac function; monitor closely. Consider testing for IgE antibodies in patients who experienced suspected allergic reactions; if positive, may be rechallenged. Pregnancy. Nursing mothers.

Pharmacological Class:

Recombinant human alpha-galactosidase A enzyme.

Adverse Reactions:

Upper RTI, chills, pyrexia, headache, cough, paresthesia, fatigue, peripheral edema, dizziness, rash; infusion reactions (discontinue if severe), anaphylaxis, allergic reactions.


Register pregnant patients at or call (800) 745-4447.

How Supplied:

Single-use vial—1

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