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ORAL CHEMOTHERAPY EDUCATION AND CEDAZURIDINE Name of your medication Generic name and cedazuridine (dehSIHtuhbeen and SEEdazYOORihdeen) Brand name Inqovi (inKOHvee)Approved uses and cedazuridine is
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Take encorafenib and binimetinib exactly as prescribed by your doctor.
02
Swallow the tablets whole with a glass of water. Do not crush, chew, or break the tablets.
03
Take the medication on an empty stomach, at least 1 hour before or 2 hours after a meal.
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Follow any special instructions given by your doctor regarding dosage adjustments or timing of doses.
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Do not stop taking the medication without consulting your doctor, even if you start to feel better.

Who needs encorafenib and binimetinib?

01
Encorafenib and binimetinib are typically prescribed for patients who have advanced melanoma that cannot be removed by surgery.
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Patients with specific genetic mutations, such as BRAF V600E or V600K, may benefit from treatment with these medications.
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Your doctor will determine if you are a suitable candidate for encorafenib and binimetinib based on your medical history and test results.
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Encorafenib and binimetinib are targeted therapies used in the treatment of certain types of cancer, specifically melanoma. Encorafenib is a BRAF inhibitor that works by blocking the BRAF protein, while binimetinib is a MEK inhibitor that targets the MEK protein, both of which are involved in cell growth and proliferation.
Healthcare providers, pharmacies, and organizations that distribute or prescribe encorafenib and binimetinib may be required to file specific information regarding their use in patient care, depending on regulatory guidelines.
Filling out encorafenib and binimetinib documentation typically involves providing patient information, dosage details, treatment duration, and compliance with regulatory forms as per local health authority requirements.
The purpose of encorafenib and binimetinib is to treat patients with BRAF V600E or V600K mutation-positive melanoma by inhibiting cancer cell growth and improving patient outcomes.
Information that must be reported includes patient demographics, treatment regimens, clinical outcomes, and any adverse reactions associated with the use of encorafenib and binimetinib.
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