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DosingDosingIBRANCE® Dosing
 
Monitoring Requirements
SafetySafetyIBRANCE® Safety ProfileNeutropeniaAdverse Event ManagementClinical Trials
Clinical TrialsIBRANCE® Clinical TrialsIBRANCE® PALOMA-2 Trial
 
IBRANCE® PALOMA-3 Trial
Real World EvidenceReal World EvidenceIBRANCE® Real World EvidenceIRIS (UK) StudyROIS
 
P-REALITY X
Patient ProfilesThe Ibrance® PatientPatient ProfilesAlison - >65 years with comorbiditiesBecky - Postmenopausal with bone-only diseaseELEVATE TVSupport and ResourcesSupport and ResourcesIBRANCE Service SupportMaterials
 
Videos

The content of this website has been produced in line with the IBRANCE® Summary of Product Characteristics for the UK. IBRANCE® (palbociclib) Prescribing Information for the UK click here.  Adverse event reporting information can be found at the bottom of the page.

The IBRANCE® Patient

IBRANCE® is indicated for the treatment of patients with HR+/HER2− locally advanced or metastatic breast cancer and is suitable for pre-, peri- or postmenopausal women. IBRANCE® can be used in combination with an AI or in combination with fulvestrant in women who have received prior endocrine therapy. For pre- or perimenopausal women, the endocrine therapy should be combined with an LHRH agonist.1​

Click for more information on the PALOMA-2 and P-REALITY X studies.

 These are fictional patients and images are illustrative only.

Profession: Teacher 

Medical History: HR+HER2- metastatic breast cancer 

Lifestyle: Active, and works full time 

Patient status: Experiences anxiety about her disease impacting her quality of life. 

What can IBRANCE do for
patients like Becky? 
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Profession: Retired nurse

Medical history: HR+HER2- breast cancer; hypertension; diabetes; atrial fibrilation; depression 

Lifestyle: Sedentary, mostly at home 

Patient status: Has difficulty performing daily tasks and maintaining a daily routine is challenging 

What can IBRANCE do for 
patients like Allison?
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ReferencesIBRANCE® (palbociclib) Summary of Product Characteristics. Available at: http://www.medicines.org.uk/emc/product/11962/smpc.
PP-IBR-GBR-6075. January 2025

Adverse events should be reported. Reporting forms and information can be found at https://yellowcard.mhra.gov.uk 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

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