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UTAH DEPARTMENT OF HEALTH, PRIOR AUTHORIZATION REQUEST FORMBraftovi (encorafenib) and Mentor (binimetinib) Member and Medication Information (required) Member ID:Member Name:DOB:Weight:Medication
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01
To fill out Braftovi Encorafenib and Mektovi, follow the instructions provided by your healthcare provider.
02
Take the prescribed dosage as directed by your doctor.
03
Braftovi and Encorafenib are usually taken together with Mektovi.
04
Follow the specific instructions regarding the timing and frequency of doses.
05
Take the medication with or without food, as instructed.
06
Swallow the tablets whole with a glass of water - do not crush, chew, or break them.
07
If you miss a dose, take it as soon as you remember.
08
Do not double the dose to make up for a missed one.
09
Continue taking Braftovi Encorafenib and Mektovi for the prescribed duration, even if you start feeling better.
10
If you have any questions or concerns regarding the medication, consult your healthcare provider.

Who needs braftovi encorafenib and mektovi?

01
Braftovi Encorafenib and Mektovi are medications used in combination to treat certain types of cancer, specifically melanoma.
02
These medications are typically prescribed to adults who have a specific genetic mutation called BRAF V600E or BRAF V600K positive advanced melanoma.
03
It is important to note that Braftovi Encorafenib and Mektovi should only be used under the supervision and prescription of a healthcare professional.
04
The eligibility for these medications may vary depending on individual circumstances, so it is best to consult with a healthcare provider to determine if you are a suitable candidate.
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Braftovi encorafenib and Mektovi are medications used to treat certain types of cancer.
Healthcare providers and facilities are required to file braftovi encorafenib and Mektovi.
Braftovi encorafenib and Mektovi should be filled out according to the guidelines provided by the medication manufacturer.
The purpose of braftovi encorafenib and Mektovi is to target specific cancer cells and inhibit their growth.
Information such as patient demographics, prescribed dosage, and treatment duration must be reported on braftovi encorafenib and Mektovi.
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