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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 for Great Britain and Northern Ireland. IBRANCE® (palbociclib) Prescribing Information for Great Britain and Northern Ireland click here. Adverse event reporting information can be found at the bottom of the page.
Confidence in a Treatment that’s setting the standard4-6
The efficacy and safety of IBRANCE® has been evaluated in two large Randomised Control Trials (RCTs) in women with HR+/HER2- metastatic Breast Cancer (mBC) as part of Pfizer’s robust PALOMA Clinical Trial Programme in Breast Cancer.2-6
IBRANCE® + Aromatase Inhibitor (AI) PALOMA-2 Clinical Trial results including efficacy and safety outcomes.
IBRANCE® + Fulvestrant (FUL) PALOMA-3 Clinical Trial results including efficacy and safety outcomes.
Real World Evidence (RWE) for IBRANCE® (pabociclib) in advanced breast cancer
IBRANCE® safety information and frequent adverse events
AI : Aromatase Inhibitor, ER+ / HER2− : Oestrogen Receptor-Positive / Human Epidermal Growth Factor Receptor 2-Negative, ET : Endocrine Therapy, HR+ / HER2- : Hormone Receptor-Positive / Human Epidermal Growth Factor Receptor 2-Negative, LHRH : Luteinising Hormone-Releasing Hormone, mBC : metastatic Breast Cancer, RCT: Randomised Controlled Trial, SmPC: Summary of Product Characteristics.
References
Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search
for MHRA Yellow Card in Google Play or Apple App Store
Adverse events should also be reported to Pfizer Medical Information on 01304 616161
To access further materials, resources and receive communication about medicines and vaccines promoted by Pfizer.
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PP-UNP-GBR-7812. January 2024