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Prescriber Criteria Formally Health Medicare Lynparza 2019 PA Fax C6957A FHC v1 120118.docx Lynparza (Clapeyron) Coverage Determination This fax machine is located in a secure location as required
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Step 1: Take the Lynparza Olaparib oral capsule at the same time each day.
02
Step 2: Swallow the capsule whole with a glass of water. Do not crush, chew, or open the capsule.
03
Step 3: You can take the capsule with or without food.
04
Step 4: If you miss a dose, take it as soon as you remember. If it is close to your next scheduled dose, skip the missed dose and continue with your regular dosing schedule. Do not take a double dose to make up for a missed one.
05
Step 5: Store the capsules at room temperature, away from heat and moisture.

Who needs lynparza olaparib oral capsule?

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Lynparza Olaparib oral capsule is typically prescribed for patients with advanced ovarian cancer, fallopian tube cancer, or primary peritoneal cancer who have received certain chemotherapy treatments and have a specific type of genetic mutation (BRCA mutation). It may also be prescribed for patients with metastatic breast cancer who have a BRCA mutation and have been previously treated with certain medications.
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Lynparza (olaparib) is an oral medication that is used as a targeted therapy for certain types of cancers, particularly those associated with BRCA mutations. It is a poly (ADP-ribose) polymerase (PARP) inhibitor that helps prevent cancer cells from repairing their DNA.
Patients prescribed Lynparza (olaparib) as part of their cancer treatment regimen are required to file their medication details with health insurance providers or healthcare systems for coverage and reimbursement.
Lynparza (olaparib) should be taken exactly as prescribed by a healthcare provider. Generally, it is taken twice daily, with or without food. Patients must follow their doctor's instructions for dosage and schedule.
The purpose of Lynparza (olaparib) is to treat certain cancers, particularly breast and ovarian cancers, by targeting cancer cells that have mutations in the BRCA genes, thereby inhibiting their ability to repair DNA.
Information that must be reported includes patient identification, prescribing physician details, dosage information, treatment duration, and any adverse effects encountered during treatment.
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