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.
Adapting Breast Cancer Care during COVID-19 pandemic
Pfizer is committed to supporting its NHS colleagues during the COVID-19 Pandemic.
NHS England has released guidance on the management of Cancer Patients at this difficult time.1 This guidance provides the following recommendations which we believe we can provide assistance with:
- Consider dispensing longer periods of oral medications if at all possible, to minimise patient exposure
- Seek alternative methods to monitor and review patients on systemic therapies.
As such, we would like to bring to your attention the availability of our 3-month packaging for IBRANCE® (palbociclib).
The 3-month packaging is available in addition to the 1-month packaging and can be ordered via the same process.
The following table provides some further useful information when ordering:
PRODUCT CODE |
PIP |
|---|---|
IBRANCE® TAB 125 mg x 63 |
416-5189 |
IBRANCE® TAB 100 mg x 63 |
416-5171 |
IBRANCE® TAB 75 mg x 63 |
416-5163 |
We can confirm that we are not making any changes to the current Patient Access scheme.
In line with our IBRANCE® Summary of Product Characteristics, for Patients who experience a maximum of Grade 1 or 2 Neutropenia in the first 6 Cycles, complete blood counts for subsequent cycles should be monitored every 3 months, prior to the beginning of a cycle and as clinically indicated.2
These patients may benefit from the 3-month packaging.
Should you require any help or assistance with necessary coding for the 3-month packaging, please contact our Customer Contact Centre on 0345 608 8866. Alternatively, you can contact your local Pfizer representative.
- NHS England. Clinical guide for the management of noncoronavirus patients requiring acute treatment: Cancer. Publications approval reference: 001559. Available at: https://www.nice.org.uk/Media/Default/About/COVID-19/Specialty-guides/cancer-and-COVID-19.pdf (accessed May 2021)
- IBRANCE® Summary of Product Characteristics for Great Britain click here. IBRANCE® Summary of Product Characteristics for Northern Ireland click here.
Resources
Materials Videos
Indication
- IBRANCE® is indicated for the treatment of HR+/HER2- locally advanced or metastatic breast cancer:
- In combination with an aromatase inhibitor; or
- In combination with fulvestrant in women who have received prior ET
In pre- or perimenopausal women, the ET should be combined with a LHRH agonist
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