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Adverse event reporting can be found at the bottom of the page
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The content of this website has been produced in line with the IBRANCE® Summary of Product Characteristics. IBRANCE® (palbociclib) Prescribing Information for the UK click here. Adverse event reporting information can be found at the bottom of the page.
Confidence Built on Evidence1-7
IBRANCE® (palbociclib) is indicated for the treatment of HR+ HER2- locally advanced or metastatic breast cancer in combination with an AI, or in combination with fulvestrant in women who have received prior endocrine therapy. In pre- or perimenopausal women, the endocrine therapy should be combined with a LHRH agonist.1
Dosing
Dosing and monitoring requirements for IBRANCE®
More information
IBRANCE® PALOMA-2 and PALOMA-3 Clinical Trial Results, including efficacy and safety outcomes
Important safety information and safety outcomes from IBRANCE® PALOMA Clinical Trials
Real-world evidence for IBRANCE® (palbociclib) in HR+ HER2- advanced Breast Cancer
View on demand content from our promotional medical education programme
AI : Aromatase Inhibitor, ET : Endocrine Therapy, HR+/HER2– : Hormone Receptor Positive / Human Epidermal Growth Factor Receptor 2 Negative, LHRH : Luteinizing Hormone-Releasing Hormone, mBC : metastatic Breast Cancer
References
Adverse events should be reported. Reporting forms and information can be found at https://yellowcard.mhra.gov.uk or search
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Adverse events should also be reported to Pfizer Medical Information on 01304 616161
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