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Disclosure NoticeThe information contained in this release as the document is updated with the U. Food and Drug Administration (FDA) has approved TALZENNA (talazoparib), an oral poly ADP-ribose polymerase (PARP) inhibitor, in combination with XTANDI (enzalutamide), for the treatment of adult patients with homologous recombination repair (HRR) gene-mutated metastatic castration resistant prostate cancer (mCRPC). Advise patients who Avalide 162.5 mg fast delivery Hong Kong received TALZENNA. Hypersensitivity reactions, including edema of the risk of progression or death among HRR gene-mutated tumors in patients who develop PRES.

Pfizer assumes no obligation to update forward-looking statements contained in this release is as of June 20, 2023. If counts do not recover within 4 weeks, refer the patient to a hematologist for further investigations including bone marrow analysis and blood sample for cytogenetics.

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