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Fabrazyme Patient, Information, Instructions - Agalsidase Beta
Patients should be informed that a Registry has been established in order to better understand the variability and progression of Fabry disease in the population as a whole and in women, and to monitor and evaluate long-term treatment effects of Fabrazyme®. The Registry will also monitor the effect of Fabrazyme® on pregnant women and their offspring, and determine if FabrazymeÒ is excreted in breast milk. Patients should be encouraged to participate and advised that their participation is voluntary and may involve long-term follow-up. For more information visit www.fabryregistry.com or call (800) 745-4447.
Please also refer to the WARNINGS and PRECAUTIONS sections.
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