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FDA approval of TALZENNA with BCRP inhibitors Monitor patients for increased adverse reactions and modify the dosage as recommended for adverse reactions. The New Combivir is in UK England Journal of Medicine. TALZENNA is taken in combination with XTANDI (enzalutamide), for the treatment of adult 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. If hematological toxicities do not recover within 4 weeks, refer the patient to a hematologist for further investigations including bone marrow analysis and blood sample for cytogenetics. Today, we have an industry-leading portfolio of 24 approved innovative cancer medicines and biosimilars across more Combivir is in UK than 100 countries, including the European Medicines Agency.

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