Understanding VIDAZA
Treatment Information for VIDAZA
Important Safety Information
Understanding Side Effects
What else you need to know
FAQs about VIDAZA
Important Safety Information
Prescribing Information
Treatment Tracker
Patient Guide
My Notepad
Educational Materials
FAQs
Side Effects
Treatment with VIDAZA
Why was VIDAZA prescribed?

VIDAZA is the first drug approved by the US Food and Drug Administration (FDA) for the treatment of all FAB subtypes of MDS. Your doctor may have prescribed VIDAZA to help reduce your need for RBC transfusions. Your doctor may prescribe VIDAZA for as long as you continue to benefit from it and side effects don’t require that you stop treatment. Always follow your doctor’s recommendations about continuing your treatment plan.

When you have MDS, your bone marrow usually makes fewer healthy blood cells. The blood cells it does make don't always work as they should.

Bone Marrow

There are different ways of classifying MDS. One system (French-American-British or FAB) divides MDS into 5 groups called subtypes. VIDAZA is used to treat patients with all 5 FAB subtypes. Your doctor can explain which subtype of MDS you have.

The 5 FAB MDS subtypes that VIDAZA treats are:

Another system (International Prognostic Scoring System or IPSS) uses cell type and blood counts of patients with MDS to predict the course of their disease. This system separates patients into lower-risk and higher-risk categories. This helps doctors determine a treatment plan for each patient.

Please see Important Safety Information and full Prescribing Information.