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Prescriber Criteria Form Marigold Rubric 2021 PA Fax 1569A V1 010121.docx Rubric (rucaparib) Coverage Determination This fax machine is located in a secure location as required by HIPAA regulations. Complete/review
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Step 1: Read the instructions and warnings provided with the Rubraca Rucaparib - Prior medication.
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Step 2: Take Rubraca Rucaparib - Prior with or without food as directed by your doctor.
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Step 3: Swallow the tablet whole with a glass of water. Do not crush, chew, or break the tablet.
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Step 4: Take Rubraca Rucaparib - Prior at the same time each day to help you remember.
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Step 5: Keep taking Rubraca Rucaparib - Prior for the prescribed duration, even if you start feeling better.
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Step 6: Contact your doctor if you experience any severe side effects or have any questions about the medication.

Who needs rubraca rucaparib - prior?

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Rubraca Rucaparib - Prior is primarily used for the treatment of advanced ovarian cancer in patients who have responded to two or more prior lines of platinum-based chemotherapy.
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It is also indicated for the maintenance treatment of recurrent ovarian cancer in patients who have shown a complete or partial response to platinum-based chemotherapy.
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Patients who have mutations in the BRCA gene may benefit from Rubraca Rucaparib - Prior treatment.
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It is important to consult with a healthcare professional to determine if Rubraca Rucaparib - Prior is appropriate for your specific condition.
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Rubraca (rucaparib) - prior is a medication used for the treatment of certain types of cancer, specifically ovarian cancer and certain types of prostate cancer.
Healthcare providers or institutions that are prescribing or administering Rubraca (rucaparib) - prior are required to file the necessary documentation.
To fill out Rubraca (rucaparib) - prior documentation, healthcare providers need to provide detailed information about the patient, the treatment plan, and any relevant medical history.
The purpose of Rubraca (rucaparib) - prior is to ensure that patients are receiving the appropriate treatment and that healthcare providers are following proper protocols.
Information that must be reported on Rubraca (rucaparib) - prior includes patient demographics, diagnosis, treatment plan, dosage, and any relevant laboratory results.
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