Genentech Ocrevus Start Form
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FDA approves 1st drug for aggressive multiple sclerosis The Spokesman
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OCREVUS® (ocrelizumab) for Relapsing MS and Primary Progressive MS
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GENENTECH INC FDA Approves Subcutaneous Formulation of Actemra for Use
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Web Patients Can Submit The Patient Consent Form Online Using The Esubmit Option.
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Ad Visit The Ocrevus® Official Physician Website For Resources To Support Your Patients.
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