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This document serves as a form to request prior approval for the prescription drug ZELBORAF (vemurafenib) for patients, requiring information from both the cardholder and the prescribing physician.
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How to fill out zelboraf
How to fill out ZELBORAF
01
Consult your healthcare provider to determine if ZELBORAF is appropriate for you.
02
Ensure you have a prescription for ZELBORAF.
03
Read the medication guide provided with your prescription thoroughly.
04
Take ZELBORAF exactly as prescribed, usually twice a day, with or without food.
05
Swallow the tablets whole with a glass of water; do not crush or chew them.
06
Keep track of your dosage schedule; try to take it at the same times each day.
07
If you miss a dose, take it as soon as you remember unless it's almost time for your next dose; do not double the dose.
08
Attend regular follow-up appointments with your healthcare provider to monitor your progress and any side effects.
Who needs ZELBORAF?
01
Patients diagnosed with metastatic melanoma that has a BRAF V600E mutation.
02
Individuals who have not responded to other treatments for their melanoma.
03
Patients who are looking for targeted therapy options for their specific cancer type.
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People Also Ask about
Is vemurafenib still used?
It is only used if the cancer cells have the BRAF V600 mutation. Vemurafenib belongs to the group of medicines called antineoplastics (cancer medicines). This medicine is available only with your doctor's prescription.
What is Zelboraf 240 mg used for?
ZELBORAF is used in adult patients to treat a type of skin cancer (unresectable or metastatic melanoma) that has a change (mutation) in the “BRAF” gene and that cannot be removed by surgery or has spread to other parts of the body.
What type of cancer can Zelboraf help cure?
Vemurafenib is a type of targeted cancer drug called a cancer growth blocker. It is a treatment for melanoma skin cancer that: can't be removed with surgery.
What does Zelboraf treat?
Zelboraf is a cancer medicine used to treat adults with melanoma (a type of skin cancer) that has spread to other parts of the body or cannot be surgically removed. Zelboraf is only for patients whose melanoma tumour cells have a specific mutation (genetic change) called 'BRAF V600'.
What is another name for Zelboraf?
vemurafenib Synonym:BRAF(V600E) kinase inhibitor RO5185426 US brand name: Zelboraf Code name: PLX4032 RG7204 RO5185426
What is the generic name for Zelboraf?
Vemurafenib. Vemurafenib (INN), sold under the brand name Zelboraf, is a medication used for the treatment of late-stage melanoma. It is an inhibitor of the B-Raf enzyme and was developed by Plexxikon.
What are the side effects of Zelboraf?
The most common side effects with Zelboraf (which may affect more than 3 in 10 patients) include arthralgia (joint pain), tiredness, rash, photosensitivity reaction (sunburn-like reactions following exposure to light), nausea and vomiting (feeling sick and being sick), alopecia (hair loss), diarrhoea, headache,
What is the generic name for Zirabev?
Zirabev () is a biosimilar to (). In general, you can think of a biosimilar medication as a generic to the original biologic. This means Zirabev () works very similarly to ().
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What is ZELBORAF?
ZELBORAF is a medication used to treat patients with melanoma that have a specific BRAF mutation.
Who is required to file ZELBORAF?
Healthcare providers and professionals who are prescribing ZELBORAF may be required to file necessary documentation for insurance or regulatory purposes.
How to fill out ZELBORAF?
Filling out ZELBORAF typically involves providing patient information, dosage details, and any required insurance codes as per the prescribing guidelines.
What is the purpose of ZELBORAF?
The purpose of ZELBORAF is to inhibit the activity of mutated BRAF proteins in cancer cells, thereby helping to slow down or stop the growth of tumors.
What information must be reported on ZELBORAF?
Information that must be reported on ZELBORAF includes patient identification details, the specific indication for use, and treatment response data.
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