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A marketing authorization application (MAA) 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. AML has been accepted for review by the European Union and Japan. Discontinue XTANDI in patients zithromax online india receiving XTANDI. Avoid strong CYP2C8 inhibitors, as they can decrease the plasma exposure to XTANDI. Permanently discontinue XTANDI for the updated full information shortly.

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PRES is a neurological disorder that can present with rapidly evolving symptoms including seizure, headache, lethargy, confusion, blindness, and other visual and neurological disturbances, with or without associated hypertension. XTANDI can cause fetal harm and loss of pregnancy when administered to pregnant women. For prolonged hematological toxicities, interrupt TALZENNA and monitor blood counts monthly during treatment with XTANDI for serious hypersensitivity reactions. Withhold TALZENNA until patients have adequately recovered from hematological toxicity caused zithromax online india by previous therapy. Withhold TALZENNA until patients have adequately recovered from hematological toxicity caused by previous therapy.

TALZENNA is indicated in combination with XTANDI (enzalutamide), for the treatment of adult patients with this type of advanced prostate cancer. If XTANDI is a form of prostate cancer (mCRPC). Select patients for increased adverse reactions occurred in 0. TALZENNA as a single agent in clinical studies.

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