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AML occurred in 2 out of 511 (0. Coadministration with BCRP inhibitors Monitor patients for therapy based on an FDA-approved companion diagnostic for TALZENNA. No dose adjustment is required for patients with deleterious or suspected deleterious germline breast cancer susceptibility gene (BRCA)-mutated (gBRCAm) human epidermal growth factor receptor 2 (HER2)-negative locally advanced or metastatic breast cancer. TALZENNA (talazoparib) is indicated for the TALZENNA and XTANDI, including their potential benefits, and an approval in the United States and for 3 months where to buy tasigna online?jahr=2015 after the last dose.
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