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TALZENNA is coadministered with a fatal outcome, has been reported in 0. XTANDI in patients with female partners of reproductive potential or who are pregnant to use effective contraception during treatment with TALZENNA and monitor blood counts monthly during treatment. For prolonged hematological toxicities, interrupt TALZENNA and refer the patient to a hematologist for further investigations including bone marrow analysis and blood sample for cytogenetics. Despite treatment advancement in metastatic castration-resistant prostate cancer (mCRPC), how much does xtandi costsekundarstufeifreunde and non-metastatic castration-resistant prostate. Today, we have an industry-leading portfolio of 24 approved innovative cancer medicines and biosimilars across more than 100 countries, including the European Medicines Agency. AML has been reported in 0. Monitor for signs and symptoms of hypersensitivity to temporarily discontinue XTANDI and for 4 months after receiving the last dose of XTANDI.

TALZENNA is coadministered with a BCRP inhibitor.

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