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Informed Consent Form A Phase II Multi institutional Study of Concurrent Radiotherapy, Palbociclib, and Hormone Therapy for Treatment of Bone Metastasis in Breast Cancer Patients NCT Number: NCT03691493Document
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01
Consult with a healthcare provider before starting concurrent use of palbociclib.
02
Follow the prescribed dosage and administration instructions given by the healthcare provider.
03
Take palbociclib at the same time each day with food, preferably breakfast.
04
Do not crush, chew, or open the capsules. Swallow them whole with a glass of water.
05
Inform the healthcare provider about any other medications or supplements being taken to avoid potential drug interactions.
06
Attend regular follow-up appointments to monitor the effectiveness and side effects of palbociclib.

Who needs concurrent use of palbociclib?

01
Patients with locally advanced or metastatic breast cancer, particularly hormone receptor-positive, human epidermal growth factor receptor 2-negative subtype, may need concurrent use of palbociclib as part of their treatment plan.
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Concurrent use of palbociclib refers to the simultaneous administration of the drug palbociclib with other medications or treatments, often as part of a comprehensive cancer treatment regimen.
Healthcare providers, including oncologists and pharmacists, who prescribe or administer palbociclib in combination with other treatments are required to file concurrent use documentation.
To fill out concurrent use documentation, providers must include patient information, details of the concurrent medications, dosage, treatment duration, and any adverse effects observed.
The purpose of concurrent use of palbociclib is to enhance the effectiveness of cancer treatment, manage disease progression, and minimize side effects by providing a holistic approach to therapy.
Reported information must include patient identity, types and doses of concurrent medications, treatment goals, monitoring results, and any adverse reactions experienced.
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