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Frequently Asked Questions

PROMACTA 

Questions and Answers for PROMACTA

Whether you’re new to PROMACTA or not, you may have questions. Here are answers to some commonly asked questions. For complete information, refer to the Medication Guide. This does not replace talking to your doctor about your medical condition or treatment. Talk with your doctor about any additional questions you may have.

PROMACTA CAN CAUSE SERIOUS SIDE EFFECTS, INCLUDING LIVER PROBLEMS. If you have chronic hepatitis C virus (HCV) and take PROMACTA with interferon and ribavirin treatment, PROMACTA may increase your risk of liver problems. Tell your doctor right away if you have any of these signs and symptoms of liver problems: yellowing of the skin or the whites of the eyes (jaundice), unusual darkening of the urine, unusual tiredness, right upper stomach area (abdomen) pain, confusion, swelling of the stomach area (abdomen). For other side effects of PROMACTA, click here.

PROMACTA is a prescription medicine used to treat people with severe aplastic anemia (SAA) when other medicines to treat your SAA have not worked well enough.

 

It is not known if PROMACTA is safe and effective in children in this disease state.

Before you take PROMACTA, tell your doctor if you:

  • Have liver or kidney problems
  • Have or had a blood clot
  • Have a history of cataracts
  • Have had surgery to remove your spleen (splenectomy)
  • Have bleeding problems
  • Are Asian and you are of Chinese, Japanese, Taiwanese, or Korean ancestry. You may need a lower dose of PROMACTA
  • Have any other medical conditions
  • Are pregnant or plan to become pregnant. It is not known if PROMACTA will harm an unborn baby
  • Are breastfeeding or plan to breastfeed. It is not known if PROMACTA passes into your breast milk. You and your healthcare provider should decide whether you will take PROMACTA or breastfeed. You should not do both

Tell your doctor about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. PROMACTA may affect the way certain medicines work. Certain other medicines may affect the way PROMACTA works.

 

Especially tell your doctor If you take:

  • Certain medicines used to treat high cholesterol, called "statins"
  • A blood thinner medicine

 

Certain medicines may keep PROMACTA from working correctly. Take PROMACTA at least 2 hours before or 4 hours after taking these products:

  • Antacids used to treat stomach ulcers or heartburn
  • Multivitamins or products that contain iron, calcium, aluminum, magnesium, selenium, and zinc, which may be found In mineral supplements

Ask your doctor If you are not sure if your medicine is one that is listed above.

 

Know the medicines you take. Keep a list of them and show it to your doctor and pharmacist when you get a new medicine.

Take PROMACTA exactly as your doctor tells you to take it. Do not stop taking PROMACTA without talking with your doctor first. Do not change your dose or schedule for taking PROMACTA unless your doctor tells you to change it. Take PROMACTA on an empty stomach, either 1 hour before or 2 hours after eating food. Take PROMACTA at least 2 hours before or 4 hours after eating dairy products and calcium fortified juices. If you miss a dose of PROMACTA, wait and take your next scheduled dose. Do not take more than one dose of PROMACTA in one day. If you take too much PROMACTA, you may have a higher risk of serious side effects. Call your doctor right away. Your doctor will check your platelet count during your treatment with PROMACTA and change your dose of PROMACTA as needed. Tell your doctor about any bruising or bleeding that happens while you take and after you stop taking PROMACTA.

Avoid situations and medicines that may increase your risk of bleeding while taking PROMACTA.

PROMACTA may cause serious side effects, including:

  • Abnormal liver function tests. Your healthcare provider will order blood tests to check your liver before you start taking PROMACTA and during your treatment. In some cases, treatment with PROMACTA may need to be stopped due to changes in your liver function tests
  • High platelet counts and a higher risk for blood clots. Your risk of getting a blood clot is increased if your platelet count is too high during treatment with PROMACTA. Your risk of getting a blood clot may also be increased during treatment with PROMACTA if you have normal or low platelet counts. You may have severe problems or die from some forms of blood clots, such as clots that travel to the lungs or that cause heart attacks or strokes. Your health care provider will check your blood platelet counts, and change your dose or stop PROMACTA if your platelet counts get too high. Tell your healthcare provider right away if you have signs and symptoms of a blood clot in the leg, such as swelling, pain, or tenderness in your leg

    People with chronic liver disease may be at risk for a type of blood clot in the stomach area. Tell your healthcare provider right away if you have stomach area pain that may be a symptom of this type of blood clot.

  • New or worsened cataracts (a clouding of the lens in the eye). New or worsened cataracts have happened in people taking PROMACTA. Your healthcare provider will check your eyes before and during your treatment with PROMACTA. Tell your healthcare provider about any changes in your eyesight while taking PROMACTA

The most common side effects of PROMACTA when used to treat severe aplastic anemia are:

  • nausea
  • feeling tired
  • cough
  • diarrhea
  • headache
  • pain in arms, legs, hands, or feet
  • shortness of breath
  • fever
  • dizziness
  • pain in the nose or throat
  • abdominal pain
  • bruising
  • muscle spasms
  • abnormal liver function tests
  • joint pain
  • runny nose

 

Laboratory tests may show abnormal changes to the cells in your bone marrow.

 

Tell your healthcare provider if you have any side effect that bothers you or that does not go away.

  • Store PROMACTA at room temperature between 68°F to 77°F (20°C to 25°C)
  • Keep PROMACTA tightly closed in the bottle given to you
  • The PROMACTA bottle may contain a desiccant pack to help keep your medicine dry. Do not remove the desiccant pack from the bottle. Keep PROMACTA and all medicines out of the reach of children

Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use PROMACTA for a condition for which it was not prescribed. Do not give PROMACTA to other people, even if they have the same symptoms that you have. It may harm them.

 

For more information about PROMACTA, go to www.PROMACTA.com or call 1-844-776-6228.

PROMACTA is a once-daily drug
 that may help boost the production of blood
 cells in your bone marrow and help treat your
 SAA. Your doctor may consider PROMACTA 
if other treatments have not worked for you.

If you miss a dose of PROMACTA, wait and take your next scheduled dose. Do not take more than one dose of PROMACTA in one day.

Take PROMACTA on an empty stomach, either 1 hour before or 2 hours after eating food. Avoid the following for at least 2 hours before or 4 hours after taking PROMACTA: dairy products, calcium-rich or magnesium-rich foods, antacids, multivitamins, supplements, or other products that contain iron, calcium, aluminum, magnesium, selenium, and zinc. These minerals may reduce your body's ability to absorb PROMACTA. Click here for a helpful meal-planning resource.

Your doctor will check your platelet count every week and change your dose of PROMACTA as needed until he/she decides that your dose of PROMACTA can stay the same. Once your doctor decides your dose can stay the same, you will need to have your platelet count checked once a month.

 

After stopping PROMACTA, your platelet count needs to be monitored weekly for at least 4 weeks to check if your platelet count drops too low.

 

Before starting PROMACTA, your liver function will be checked through blood tests. During dose adjustments, it will be tested every 2 weeks, transitioning to monthly tests once your dose can stay the same. In some cases, treatment with PROMACTA may need to be stopped due to changes in your liver function tests.

Information and organizations related to SAA

Additionally, there are many resources available to help you learn more about SAA and connect with others who are living with this condition.

 

Aplastic Anemia & MDS International Foundation

www.aamds.org

Dedicated to supporting patients and families living with aplastic anemia and related diseases of bone marrow failure.

 

American Society of Hematology

www.hematology.org

Furthering the understanding, diagnosis, treatment, and prevention of certain blood and bone disorders.

 

National Heart, Lung, and Blood Institute (NHLBI)

www.nhlbi.nih.gov

NHLBI promotes the prevention and treatment of heart, lung, and blood diseases.

 

The organizations and websites listed on this page are maintained by third parties over whom Novartis Pharmaceuticals Corporation has no control. As such, Novartis Pharmaceuticals Corporation makes no representation as to the accuracy or any other aspect of the information supplied by these organizations or contained in these websites.