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Click here for BOSULIF® (bosutinib) Prescribing Information. Adverse event reporting information can be found at the bottom of the page.
400 mg BOSULIF once daily for adult patients with newly diagnosed chronic phase (CP) Philadelphia chromosome–positive chronic myelogenous leukemia (Ph+ CML)
Dose escalation or reduction by 100mg may be considered depending on patients response and tolerability. Doses greater than 600 mg/day have not been studied and, therefore, should not be given. Doses less than 300 mg/day have been used in patients; however, efficacy has not been established.
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Adverse events should be reported. Report an adverse event to your national reporting system (HPRA Pharmacovigilance)
Adverse events should also be reported to Pfizer Medical Information on 1800 633 363
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PP-UNP-IRL-0176. January 2023