Resources for Care Partners | Rubraca® (rucaparib) tablets
Caregiver
Caregiver

Care partners play an important role

As a care partner, you are a central part of your loved one’s treatment journey. Here are some of the ways you can help her while she’s taking Rubraca. You’ll also see tips to help you take care of yourself during this time, which is very important. You’ll find it much easier to help if you’re taking the time to tend to yourself.

How to be prepared

prepared
  • Asking a member of the oncology healthcare team for recommendations of where to go to research ovarian cancer and Rubraca
  • Taking notes, and asking a member of the oncology healthcare team to clarify questions
  • Finding out where to turn if there is an emergency: who to call, and how to reach them

How to be there

Be There
  • Going to oncologist visits together
    • Making a list of questions before the visit
    • Encouraging your loved one to feel confident discussing any concerns she has with her oncology healthcare team. Consider mentioning any concerns or questions that she may be uncomfortable bringing up
    • Speaking up if there is anything you don’t understand
  • Taking the time to listen when your loved one needs to talk
  • Offering to run errands and/or help with additional housekeeping chores

How to be organized

Organize
  • Keeping track of important papers
    • Picking one place to keep all medical reports, insurance claims, and other healthcare documents
    • Storing information in a place that’s easy to remember and access
    • Using a binder and/or filing cabinet

How to be healthy

Healthy
  • Making self-care a priority
  • Staying healthy—exercising as regularly as you can, eating a balanced diet, and remembering to go to your doctor's appointments
  • Joining a support group for care partners
  • Setting aside time to do an activity you enjoy, such as reading a book, watching your favorite TV show, or going for a bike ride

Learn about helpful support and resources for Rubraca

Connections Learn more

Discover how Rubraca may help maintain the response to platinum-based chemotherapy

Trial Results Learn more

Find out about the possible side effects of Rubraca

Side Effects Learn more

INDICATIONS

What is Rubraca?

Rubraca® (rucaparib) tablets are a prescription medicine used for:

  • the maintenance treatment of adults with ovarian cancer, fallopian tube cancer, or primary peritoneal cancer whose cancer has come back and who are in response (complete or partial response) to a platinum-based chemotherapy
  • the treatment of adults with ovarian cancer, fallopian tube cancer, or primary peritoneal cancer who have certain “BRCA” gene mutations, either inherited (germline) or acquired (somatic), and who have been treated with 2 or more chemotherapy medicines for their cancer. Your healthcare provider will perform a test to make sure Rubraca is right for you

It is not known if Rubraca is safe and effective in children. 

SELECT IMPORTANT SAFETY INFORMATION

Read full

warning Rubraca tablets may cause serious side effects including bone marrow problems called Myelodysplastic Syndrome (MDS) or a type of cancer of the blood called Acute Myeloid Leukemia (AML). Some people who have ovarian cancer and who have received previous treatment with chemotherapy or certain other medicines for their cancer have developed MDS or AML during or after treatment with Rubraca. MDS or AML may lead to death. If you develop MDS or AML, your healthcare provider will stop treatment with Rubraca.

warning Symptoms of low blood cell counts are common during treatment with Rubraca but can be a sign of serious problems, including MDS or AML. Tell your healthcare provider if you have any of the following symptoms during treatment with Rubraca:

  • weakness
  • weight loss
  • fever
  • frequent infections
  • blood in urine or stool
  • shortness of breath
  • feeling very tired
  • bruising or bleeding more easily

warning Your healthcare provider will do blood tests before, and every month during treatment with Rubraca to monitor your blood cell counts. Weekly blood tests will be performed if you have low blood cell counts for a long time. Your healthcare provider may stop treatment with Rubraca until your blood cell counts improve. 

warning Before you take Rubraca, tell your healthcare provider about all of your medical conditions, including if you:

warning

  • are pregnant or plan to become pregnant. Rubraca can harm your unborn baby and may cause loss of pregnancy (miscarriage). You should not become pregnant during treatment with Rubraca.
    • If you are able to become pregnant, your healthcare provider may do a pregnancy test before you start treatment with Rubraca.
    • Females who are able to become pregnant should use effective birth control during treatment and for at least 6 months after receiving the last dose of Rubraca.
    • Talk to your healthcare provider about birth control methods that may be right for you.
    • Tell your healthcare provider right away if you become pregnant.

warning

  • are breastfeeding or plan to breastfeed. It is not known if Rubraca passes into breast milk. Do not breastfeed during treatment and for 2 weeks after the last dose of Rubraca. Talk to your healthcare provider about the best way to feed your baby during this time.

warning Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. 

warning  While taking Rubraca, avoid spending time in sunlight.  Rubraca can make your skin sensitive to the sun (photosensitivity).  You may burn more easily during treatment with Rubraca. You should wear a hat and clothes that cover your skin and use sunscreen to help protect against sunburn if you have to be in the sunlight.

warning The most common side effects of Rubraca include:

  • nausea 
  • tiredness or weakness
  • vomiting
  • decrease in hemoglobin (anemia)
  • changes in how food tastes
  • constipation
  • decrease in appetite 
  • diarrhea
  • low blood cell counts
  • mouth sores
  • upper respiratory tract infection
  • shortness of breath
  • rash
  • changes in liver or kidney function blood tests
  • stomach (abdomen) pain
  • increased cholesterol levels

warning These are not all of the possible side effects of Rubraca. For more information, ask your healthcare provider or pharmacist. Call your healthcare provider for medical advice about side effects.

warning  You may report side effects to the FDA at 1‑800‑FDA‑1088 or www.fda.gov/medwatch. You may also report side effects to Clovis Oncology, Inc. at 1‑415‑409‑7220 (US toll) or 1‑844‑CLVS‑ONC (1‑844‑258‑7662; US toll-free).

Please see full Prescribing Information, including Patient Information, for additional Important Safety Information.

INDICATIONS

What is Rubraca?

Rubraca® (rucaparib) tablets are a prescription medicine used for:

  • the maintenance treatment of adults with ovarian cancer, fallopian tube cancer, or primary peritoneal cancer whose cancer has come back and who are in response (complete or partial response) to a platinum-based chemotherapy
  • the treatment of adults with ovarian cancer, fallopian tube cancer, or primary peritoneal cancer who have certain “BRCA” gene mutations, either inherited (germline) or acquired (somatic), and who have been treated with 2 or more chemotherapy medicines for their cancer. Your healthcare provider will perform a test to make sure Rubraca is right for you

It is not known if Rubraca is safe and effective in children. 

SELECT IMPORTANT SAFETY INFORMATION

Read full

warning Rubraca tablets may cause serious side effects including bone marrow problems called Myelodysplastic Syndrome (MDS) or a type of cancer of the blood called Acute Myeloid Leukemia (AML). Some people who have ovarian cancer and who have received previous treatment with chemotherapy or certain other medicines for their cancer have developed MDS or AML during or after treatment with Rubraca. MDS or AML may lead to death. If you develop MDS or AML, your healthcare provider will stop treatment with Rubraca.

warning Symptoms of low blood cell counts are common during treatment with Rubraca but can be a sign of serious problems, including MDS or AML. Tell your healthcare provider if you have any of the following symptoms during treatment with Rubraca:

  • weakness
  • weight loss
  • fever
  • frequent infections
  • blood in urine or stool
  • shortness of breath
  • feeling very tired
  • bruising or bleeding more easily

warning Your healthcare provider will do blood tests before, and every month during treatment with Rubraca to monitor your blood cell counts. Weekly blood tests will be performed if you have low blood cell counts for a long time. Your healthcare provider may stop treatment with Rubraca until your blood cell counts improve. 

warning Before you take Rubraca, tell your healthcare provider about all of your medical conditions, including if you:

warning

  • are pregnant or plan to become pregnant. Rubraca can harm your unborn baby and may cause loss of pregnancy (miscarriage). You should not become pregnant during treatment with Rubraca.
    • If you are able to become pregnant, your healthcare provider may do a pregnancy test before you start treatment with Rubraca.
    • Females who are able to become pregnant should use effective birth control during treatment and for at least 6 months after receiving the last dose of Rubraca.
    • Talk to your healthcare provider about birth control methods that may be right for you.
    • Tell your healthcare provider right away if you become pregnant.

warning

  • are breastfeeding or plan to breastfeed. It is not known if Rubraca passes into breast milk. Do not breastfeed during treatment and for 2 weeks after the last dose of Rubraca. Talk to your healthcare provider about the best way to feed your baby during this time.

warning Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. 

warning  While taking Rubraca, avoid spending time in sunlight.  Rubraca can make your skin sensitive to the sun (photosensitivity).  You may burn more easily during treatment with Rubraca. You should wear a hat and clothes that cover your skin and use sunscreen to help protect against sunburn if you have to be in the sunlight.

warning The most common side effects of Rubraca include:

  • nausea 
  • tiredness or weakness
  • vomiting
  • decrease in hemoglobin (anemia)
  • changes in how food tastes
  • constipation
  • decrease in appetite 
  • diarrhea
  • low blood cell counts
  • mouth sores
  • upper respiratory tract infection
  • shortness of breath
  • rash
  • changes in liver or kidney function blood tests
  • stomach (abdomen) pain
  • increased cholesterol levels

warning These are not all of the possible side effects of Rubraca. For more information, ask your healthcare provider or pharmacist. Call your healthcare provider for medical advice about side effects.

warning  You may report side effects to the FDA at 1‑800‑FDA‑1088 or www.fda.gov/medwatch. You may also report side effects to Clovis Oncology, Inc. at 1‑415‑409‑7220 (US toll) or 1‑844‑CLVS‑ONC (1‑844‑258‑7662; US toll-free).

Please see full Prescribing Information, including Patient Information, for additional Important Safety Information.