Eltrombopag Olamine – Uses, Dosage, Side Effects, Interaction

Eltrombopag Olamine is the orally active ethanolamine salt of eltrombopag, a small-molecule, nonpeptide thrombopoietin receptor agonist with megakaryopoiesis-stimulating activity. Eltrombopag binds to and stimulates the transmembrane domain of the platelet thrombopoietin receptor (TPO-R or CD110), a member of the hematopoietic receptor superfamily. Activation of TPO-R leads to the proliferation and differentiation of cells in the megakaryocytic lineage and an increase in platelet production.

Mechanism of Action

Eltrombopag is an orally bioavailable, small-molecule TPO-receptor agonist that interacts with the transmembrane domain of the human TPO-receptor. Eltrombopag is a stimulator of STAT and JAK phosphorylation. Unlike recombinant TPO or romiplostim, Eltrombopag does not activate the AKT pathway in any way. It should be noted that when given to patients with aplastic anemia, other lineages besides platelet count were increased, suggesting that either eltrombopag enhanced the effect of TPO in vivo; or there is a yet uncovered mechanism of action at work.

Eltrombopag is an orally bioavailable, small-molecule thrombopoietin (TPO)-receptor agonist that interacts with the transmembrane domain of the human TPO-receptor and initiates signaling cascades that induce proliferation and differentiation from bone marrow progenitor cells.

Indications

  • Thrombopoietin receptor agonists are pharmaceutical agents that stimulate platelet production in the bone marrow. In this, they differ from the previously discussed agents that act by attempting to curtail platelet destruction.
  • Eltrombopag is indicated for the treatment of adult patients with primary immune thrombocytopenia (ITP) who are refractory to other treatments (e. g. corticosteroids, and immunoglobulins).
  • Eltrombopagis indicated for the treatment of pediatric patients aged 1 year and above with primary immune thrombocytopenia (ITP) lasting 6 months or longer from diagnosis and who are refractory to other treatments (e. g. corticosteroids, immunoglobulins).
  • Eltrombopag is indicated in adult patients with chronic hepatitis C virus (HCV) infection for the treatment of thrombocytopenia, where the degree of thrombocytopenia is the main factor preventing the initiation or limiting the ability to maintain optimal interferon-based therapy.
  • Eltrombopag is indicated in adult patients with acquired severe aplastic anemia (SAA) who were either refractory to prior immunosuppressive therapy or heavily pretreated and are unsuitable for hematopoietic stem cell transplantation
  • Eltrombopag is indicated for the treatment of thrombocytopenia in patients with chronic immune (idiopathic) thrombocytopenia (ITP) who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy.
  • Eltrombopag is indicated for the treatment of thrombocytopenia in patients with chronic hepatitis C to allow the initiation and maintenance of interferon-based therapy.
  • Eltrombopag is indicated for the treatment of patients with severe aplastic anemia who have had an insufficient response to immunosuppressive therapy.
  • Eltrombopag should be used only in patients with immune (idiopathic) thrombocytopenia (ITP) whose degree of thrombocytopenia and clinical condition increases the risk for bleeding. Promacta should be used only in patients with chronic hepatitis C whose degree of thrombocytopenia prevents the initiation of interferon-based therapy or limits the ability to maintain interferon-based therapy. Safety and efficacy have not been established in combination with direct-acting antiviral agents used without interferon for the treatment of chronic hepatitis C infection.
  •  In combination with standard immunosuppressive therapy as first-line treatment of patients with severe aplastic anemia.

Use in Cancer.

Eltrombopag olamine is approved to treat:

  • Thrombocytopenia (low platelet levels). It is used in adults and in children aged 1 year or older with chronic immune thrombocytopenia (ITP). ITP is a condition in which platelets are destroyed by the immune system. Eltrombopag olamine is used in certain patients with ITP who have not gotten better with other treatments.

Eltrombopag olamine is also being studied in the treatment of other conditions and types of cancer.

Contraindications

  • increase in the number of platelets in the blood
  • clouding of the lens of the eye called cataracts
  • obstruction of a blood vessel by a blood clot
  • a blood clot in a vein of the liver
  • at risk for formation of blood clots
  • acute liver failure
  • damage to the liver and inflammation
  • decreased kidney function
  • high amount of bilirubin in the blood
  • abnormal liver function tests
  • a patient who is producing milk and breastfeeding
  • antiphospholipid antibody syndrome
  • abnormal blood clotting due to factor V leiden mutation
  • hereditary antithrombin III deficiency
  • Child-Pugh class A liver impairment
  • Child-Pugh class B liver impairment
  • Child-Pugh class C liver impairment

Dosage

Strengths: 25 mg; 50 mg; 75 mg; 12.5 mg

Aplastic Anemia

FIRST-LINE SEVERE APLASTIC ANEMIA:

  • Initial dose: 150 mg orally once a day

Patients of Asian Ancestry (such as Chinese, Japanese, Taiwanese, Korean, or Thai):

  • Initial dose: 75 mg orally once a day
  • Duration of therapy: 6 months
  • If baseline ALT or AST levels are greater than 6 times the upper limit of normal (ULN), do not initiate this drug until transaminase levels are less than 5 x ULN.
  • Initiate this drug concurrently with standard immunosuppressive therapy.
  • Do not exceed the initial dose.

REFRACTORY SEVERE APLASTIC ANEMIA:

  • Initial dose: 50 mg orally once a day; may adjust the dose in 50 mg increments every 2 weeks as needed to achieve a platelet count between 50 and 200 x 10(9)/L.
  • Initial dose: 25 mg orally once a day; may adjust the dose in 50 mg increments every 2 weeks as needed to achieve a platelet count between 50 and 200 x 10(9)/L.
  • Maintenance dose: The lowest dose needed to achieve and maintain a platelet count between 50 and 200 x 10(9)/L.
  • Maximum dose: 150 mg orally once a day
  • Duration of therapy: If no hematologic response has occurred after 16 weeks of therapy with this drug, discontinue therapy.
  • For patients who achieve trilineage response, including transfusion independence, lasting at least 8 weeks, the dose of this drug may be reduced by 50%. If counts remain stable after 8 weeks at the reduced dose, then this drug may be discontinued. If platelet counts drop to less than 30 x 10(9)/L, hemoglobin to less than 9 g/dL, or absolute neutrophil count (ANC) to less than 0.5 x 10(9)/L, this drug may be reinitiated at the previous effective dose
  • If new cytogenetic abnormalities are observed, consider discontinuation of this drug.

Idiopathic (Immune) Thrombocytopenic Purpura

  • Initial dose: 50 mg orally once a day
  • Initial dose: 25 mg orally once a day
  • Maintenance dose: The lowest dose to achieve and maintain a platelet count between 50 to 200 x 10(9)/L as necessary to reduce the risk of bleeding.
  • Maximum dose: 75 mg orally once a day
  • Duration: Treatment should be discontinued if the platelet count does not increase to a level sufficient to avoid clinically important bleeding after 4 weeks of therapy at the maximum daily dose.
  • Monitor CBC with differentials, including platelet counts, every week until the platelet count is stable, followed by monthly thereafter. Monitoring should continue every week for at least 4 weeks following treatment discontinuation.
  • Platelet counts generally increase within 1 to 2 weeks after starting therapy and decrease within 1 to 2 weeks after treatment discontinuation.

Thrombocytopenia

  • Initial dose: 25 mg orally once a day
  • Maintenance dose: The lowest dose to achieve and maintain a platelet count necessary to initiate and maintain antiviral therapy with pegylated interferon and ribavirin.
  • Maximum dose: 100 mg orally once a day
  • Duration: Treatment should be discontinued when concomitant antiviral therapy is discontinued
  • Adjust the daily dose by increments of 25 mg every two weeks as necessary according to platelet count response.
  • Monitor platelet counts every week prior to starting antiviral therapy.
  • During antiviral therapy, monitor CBC with differentials, including platelet counts, every week until the platelet count is stable. Monitor platelet counts monthly thereafter.
  • Platelet counts generally begin to rise within the first week of treatment with eltrombopag.
  • Treatment of thrombocytopenia in patients with chronic hepatitis C to allow the initiation and maintenance of interferon-based therapy.

Pediatric Dose

Idiopathic (Immune) Thrombocytopenic Purpura

1 TO 5 YEARS:

  • Initial dose: 25 mg orally once a day

6 YEARS OR OLDER:

  • Initial dose: 50 mg orally once a day
  • Initial dose: 25 mg orally once a day
  • Maintenance dose: The lowest dose to achieve and maintain a platelet count between 50 to 200 x 10(9)/L as necessary to reduce the risk of bleeding.
  • Maximum dose: 75 mg orally once a day
  • Duration: Treatment should be discontinued if the platelet count does not increase to a level sufficient to avoid clinically important bleeding after 4 weeks of therapy at the maximum daily dose.
  • Monitor CBC with differentials, including platelet counts, every week until the platelet count is stable, followed by monthly thereafter. Monitoring should continue every week for at least 4 weeks following treatment discontinuation.
  • Platelet counts generally increase within 1 to 2 weeks after starting therapy and decrease within 1 to 2 weeks after treatment discontinuation.

Aplastic Anemia

FIRST-LINE SEVERE APLASTIC ANEMIA:
Initial dose:

  • 2 to 5 years: 2.5 mg/kg orally once a day
  • 6 to 11 years: 75 mg orally once a day
  • 12 years or older: 150 mg orally once a day

Patients of Asian ancestry (such as Chinese, Japanese, Taiwanese, Korean, or Thai):
Initial dose:

  • 2 to 5 years: 1.25 mg/kg orally once a day
  • 6 to 11 years: 37.5 mg orally once a day
  • 12 years or older: 75 mg orally once a day
  • Duration of therapy: 6 months
  • If baseline ALT or AST levels are greater than 6 times the upper limit of normal (ULN), do not initiate this drug until transaminase levels are less than 5 x ULN.
  • Initiate this drug concurrently with standard immunosuppressive therapy.
  • Do not exceed the initial dose.

Liver Dose Adjustments

CHRONIC IMMUNE THROMBOCYTOPENIA:

  • Mild to severe liver dysfunction (Child-Pugh A, B, or C): Initiate dose at 25 mg orally once a day
  • Mild to severe liver dysfunction with East Asian ancestry: Initiate dose at 12.5 mg orally once a day
  • In patients with liver dysfunction (Child-Pugh Class A, B, C), after initiating eltrombopag or after any subsequent dosing increase, wait 3 weeks before increasing the dose.

CHRONIC HEPATITIS C-ASSOCIATED THROMBOCYTOPENIA:

  • Liver dysfunction: No dosage adjustment is recommended

FIRST-LINE SEVERE APLASTIC ANEMIA:

  • If baseline ALT or AST levels are greater than 6 times the upper limit of normal (ULN), do not initiate this drug until transaminase levels are less than 5 x ULN.

Mild to Severe Liver Dysfunction (Child-Pugh A, B, or C):
Initial dose:

  • 2 to 5 years: 1.25 mg/kg orally once a day for 6 months
  • 6 to 11 years: 37.5 mg orally once a day for 6 months
  • 12 years or older: 75 mg orally once a day for 6 months
  • Increase in ALT or AST greater than 6 x ULN: Discontinue this drug. Once ALT or AST is less than 5 x ULN, reinitiate this drug at the same dose.
  • Increase in ALT or AST greater than 6 x ULN after reinitiating this drug: Discontinue this drug and monitor ALT or AST at least every 3 to 4 days. Once ALT or AST is less than 5 x ULN, reinitiate this drug at a daily dose reduced by 25 mg compared to the previous dose.
  • If ALT or AST returns to greater than 6 x ULN on the reduced dose: Reduce the daily dose of this drug by 25 mg until ALT or AST is less than 5 x ULN. In pediatric patients, less than 12 years of age, reduce the daily dose by at least 15% to the nearest dose that can be administered.

REFRACTORY SEVERE APLASTIC ANEMIA:
Mild to Severe Liver Dysfunction (Child-Pugh A, B, or C):

  • Initial dose: 25 mg orally once a day

GENERAL:
Discontinue eltrombopag if ALT levels increase by at least 3 x ULN in patients with normal liver function or transaminases increase by at least 3 x baseline levels in patients with elevated transaminases pretreatment and where transaminases are:

  • Progressively increasing,
  • Persistent for at least 4 weeks,
  • Accompanied by increased direct bilirubin, or
  • Accompanied by clinical symptoms of liver injury or evidence of hepatic decompensation
  • Treatment may be cautiously restarted if the benefits outweigh the risks, with weekly LFT monitoring during the dose adjustment phase; however, it should be permanently discontinued if LFT abnormalities remain, worsen, or reoccur.

Dose Adjustments

General:

  • A period of at least 2 weeks is recommended between dose adjustments in order to see the effect on the platelet count.
  • Excessive platelet count responses necessitate eltrombopag treatment discontinuation.

Thrombocytopenia in Patients with Chronic ITP:

  • General: Modify the dosage regimen of concomitant ITP medications, as medically appropriate, to avoid
    excessive increases in platelet counts during eltrombopag therapy.

Platelet count:

  • Less than 50 x 10(9)/L following at least 2 weeks of eltrombopag therapy: Increase daily dose by 25 mg to a maximum of 75 mg per day. For patients taking 12.5 mg once a day, increase the dose to 25 mg once a day before increasing the dose amount by 25 mg.
  • Greater than or equal to 200 x 10(9)/L to less than or equal to 400 x 10(9)/L at any time: Decrease the daily dose by 25 mg. For patients taking 25 mg once a day, decrease the dose to 12.5 mg once a day.
  • Greater than 400 x 10(9)/L: Stop eltrombopag; increase platelet monitoring to twice weekly. Once the platelet count is less than 150 x 10(9)/L, restart eltrombopag at a daily dose reduced by 25 mg. For patients taking 25 mg once a day, restart therapy at 12.5 mg once a day.
  • Greater than 400 x 10(9)/L after 2 weeks of therapy at the lowest dose of eltrombopag: Discontinue eltrombopag

Thrombocytopenia in Patients with Chronic Hepatitis C:
General:

  • During antiviral therapy, the dose of eltrombopag should be adjusted to avoid dose reductions of peginterferon.
  • Eltrombopag should be discontinued when antiviral therapy is discontinued.

Platelet count:

  • Less than 50 x 10(9)/L following at least 2 weeks of eltrombopag therapy: Increase daily dose by 25 mg to a maximum of 100 mg per day
  • Greater than or equal to 200 x 10(9)/L to less than or equal to 400 x 10(9)/L at any time: Decrease the daily dose by 25 mg
  • Greater than 400 x 10(9)/L: Stop eltrombopag; increase platelet monitoring to twice weekly. Once the platelet count is less than 150 x 10(9)/L, restart eltrombopag at a daily dose reduced by 25 mg. For patients taking 25 mg once a day, restart therapy at 12.5 mg once a day.
  • Greater than 400 x 10(9)/L after 2 weeks of therapy at the lowest dose of eltrombopag: Discontinue eltrombopag

First-line Severe Aplastic Anemia:
Platelet count:

  • Greater than 200 x 10(9)/L to less than or equal to 400 x 10(9)/L: Decrease the daily dose by 25 mg every 2 weeks to the lowest dose that maintains a platelet count of at least 50 x 10(9)/L. In pediatric patients less than 12 years of age, decrease the dose by 12.5 mg.
  • Greater than 400 x 10(9)/L: Discontinue this drug for 1 week. Once the platelet count is less than 200 x 10(9)/L, reinitiate this drug at a daily dose reduced by 25 mg (or 12.5 mg in pediatric patients less than 12 years of age).

Thromboembolic events (e.g., deep vein thrombosis, pulmonary embolus, stroke, myocardial infarction): Discontinue this drug but remain on horse anti-thymocyte globulin (h-ATG) and cyclosporine.

Refractory Severe Aplastic Anemia:

Platelet count:

  • Less than 50 x 10(9)/L following at least 2 weeks of this drug: Increase daily dose by 50 mg to a maximum of 150 mg/day. For patients taking 25 mg once a day, increase the dose to 50 mg once a day before increasing the dose amount by 50 mg.
  • Greater than or equal to 200 x 10(9)/L to less than or equal to 400 x 10(9)/L at any time: Decrease the daily dose by 50 mg.
  • Greater than 400 x 10(9)/L: Stop this drug for 1 week. Once the platelet count is less than 150 x 10(9)/L, reinitiate therapy at a dose reduced by 50 mg.
  • Greater than 400 x 10(9)/L after 2 weeks of therapy at the lowest dose of this drug: Discontinue this drug.

Administration advice:

  • This drug should be taken without a meal or with a meal low in calcium (50 mg or less) and at least 2 hours before or 4 hours after other medications (e.g., antacids), calcium-rich foods, or supplements containing polyvalent cations such as iron, calcium, aluminum, magnesium, selenium, and zinc.
  • Do not administer more than one dose of eltrombopag within any 24-hour period.
  • Do not split, chew, or crush tablets and mix them with food or liquids.

Side Effects

The Most Common

  • back pain
  • muscle aches or spasms
  • headache
  • flu symptoms such as fever, headache, sore throat, cough, tiredness, chills, and body aches
  • weakness
  • extreme tiredness
  • decreased appetite
  • pain or swelling in the mouth or throat
  • hair loss
  • rash
  • skin color changes
  • skin tingling, itching, or burning
  • swelling of the ankles, feet, or lower legs
  • toothache (in children)
  • swelling, pain, tenderness, warmth or redness in one leg
  • shortness of breath, coughing up blood, fast heartbeat, fast breathing, pain when breathing deeply
  • pain in the chest, arms, back, neck, jaw, or stomach, breaking out in cold sweat, lightheadedness
  • slow or difficult speech, sudden weakness or numbness of the face, arm or leg, sudden headache, sudden vision problems, sudden difficulty walking
  • stomach pain, nausea, vomiting, diarrhea
  • cloudy, blurry vision, or other vision changes

More common

  • Bloating or swelling of the face, arms, hands, lower legs, or feet
  • body aches or pain
  • chills
  • cough
  • difficulty with breathing
  • fever
  • headache
  • loss of voice
  • pain in the chest, groin, or legs, especially the calves
  • pale skin
  • rapid weight gain
  • runny nose
  • severe, sudden headache
  • slurred speech
  • sore throat
  • sudden loss of coordination
  • sudden, severe weakness or numbness in the arm or leg
  • tingling of the hands or feet
  • troubled breathing with exertion
  • unusual tiredness or weakness
  • unusual weight gain or loss
  • yellow eyes or skin
  • Decreased appetite
  • difficulty with moving
  • hair loss or thinning of the hair
  • itching skin
  • lack or loss of strength
  • muscle cramps or stiffness
  • swollen joints

Rare

  • Bladder pain
  • blindness
  • blurred or decreased vision
  • bruising
  • burning, crawling, itching, numbness, prickling, “pins and needles”, or tingling feelings
  • diarrhea
  • a general feeling of discomfort or illness
  • hoarseness
  • joint pain
  • lower back or side pain
  • muscle aches and pains
  • nausea
  • pinpoint red spots on the skin
  • redness of the eye
  • shivering
  • sweating
  • tender, swollen glands in the neck
  • trouble sleeping
  • trouble swallowing
  • voice changes
  • vomiting
  • Back pain
  • belching
  • bone pain
  • darkening of the skin
  • dry mouth
  • heartburn
  • indigestion
  • rash
  • stomach discomfort, upset, or pain

Drug Interactions

Pregnancy and Lactation

FDA Pregnancy Category C

Pregnancy

There are no adequate and well-controlled studies of eltrombopag use in pregnancy. In animal reproduction and developmental toxicity studies, there was evidence of embryolethality and reduced fetal weights at maternally toxic doses. PROMACTA should be us

Lactation

It is not known whether eltrombopag is excreted in human milk. Because many drugs are excreted in human milk and because of the potential for serious adverse reactions in nursing infants from PROMACTA, a decision should be made whether to discontinue nursing or to
discontinue PROMACTA taking into account the importance of PROMACTA to the mother and the known benefits of nursing.

How should this medicine be used?

Eltrombopag comes as a tablet and as a powder for oral suspension (liquid) to take by mouth. It is usually taken once a day on an empty stomach, at least 1 hour before or 2 hours after eating. Take eltrombopag at around the same time every day. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take eltrombopag exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor.

Take eltrombopag at least 2 hours before or 4 hours after you eat or drink foods that contain a lot of calcium, such as dairy products, calcium-fortified juices, cereals, oatmeal, and bread; trout; clams; leafy green vegetables such as spinach and collard greens; and tofu and other soy products. Ask your doctor if you are not sure if a food contains a lot of calcium. You may find it helpful to take eltrombopag close to the beginning or end of your day so that you will be able to eat these foods during most of your waking hours.

Swallow the tablets whole. Do not split, chew, or crush them and mix them into food or liquids.

If you are taking the powder for oral suspension, carefully read the manufacturer’s instructions for use that comes with the medication. These instructions describe how to prepare and measure your dose. Mix the powder with cool or cold water before use. Do not mix the powder with hot water. Immediately after preparation, swallow the dose. If it is not taken within 30 minutes or if there is remaining liquid, dispose of the mixture in the trash (do not pour it down the sink).

Do not allow the powder to touch your skin. If you spill the powder on your skin, wash it off immediately with soap and water. Call your doctor if you have a skin reaction or if you have any questions.

Your doctor will probably start you on a low dose of eltrombopag and adjust your dose depending on your response to the medication. At the beginning of your treatment, your doctor will order a blood test to check your platelet level once every week. Your doctor may increase your dose if your platelet level is too low. If your platelet level is too high, your doctor may decrease your dose or may not give you eltrombopag for a time. After your treatment has continued for some time and your doctor has found the dose of eltrombopag that works for you, your platelet level will be checked less often. Your platelet level will also be checked weekly for at least 4 weeks after you stop taking eltrombopag.

If you have chronic ITP, you may receive other medications to treat your condition along with eltrombopag. Your doctor may decrease your dose of these medications if eltrombopag works well for you.

Eltrombopag does not work for everyone. If your platelet level does not increase enough after you have taken eltrombopag for some time, your doctor may tell you to stop taking eltrombopag.

Eltrombopag may help to control your condition but will not cure it. Continue to take eltrombopag even if you feel well. Do not stop taking eltrombopag without talking to your doctor.

What special precautions should I follow?

Before taking eltrombopag,

  • tell your doctor and pharmacist if you are allergic to eltrombopag, any other medications, or any of the ingredients in eltrombopag tablets. Ask your pharmacist or check the Medication Guide for a list of the ingredients.
  • tell your doctor and pharmacist what prescription and nonprescription medications, vitamins, nutritional supplements, and herbal products you are taking or plan to take. Be sure to mention any of the following: anticoagulants (blood thinners) such as warfarin (Coumadin, Jantoven); bosentan (Tracleer); cholesterol-lowering medications (statins) such as atorvastatin (Lipitor, in Caduet), fluvastatin (Lescol), pitavastatin (Livalo, Zypitamag), pravastatin (Pravachol), rosuvastatin (Crestor), and simvastatin (Zocor, Flolopid, in Vytorin); ezetimibe (Zetia, in Vytorin); glyburide (Diabeta, Glynase); imatinib (Gleevec); irinotecan (Camptosar, Onivyde); olmesartan (Benicar, in Azor, in Tribenzor); lapatinib (Tykerb); methotrexate (Rasuvo, Trexall, others); mitoxantrone; repaglinide (Prandin): rifampin (Rimactane, Rifadin, in Rifamate, Rifater); sulfasalazine (Azulfidine); topotecan (Hycamtin), and valsartan (Diovan, in Byvalson, in Entresto, in Exforge). Your doctor may need to change the doses of your medications or monitor you carefully for side effects. Many other medications may also interact with eltrombopag, so be sure to tell your doctor about all the medications you are taking, even those that do not appear on this list.
  • if you are taking antacids containing calcium, aluminum, or magnesium (Maalox, Mylanta, Tums) or vitamin or mineral supplements containing calcium, iron, zinc or selenium, take eltrombopag 2 hours before or 4 hours after you take them.
  • tell your doctor if you are of East Asian (Chinese, Japanese, Taiwanese, or Korean) descent and if you have or have ever had a cataract (clouding of the lens of the eye that may cause vision problems), blood clots, any condition that increases the risk that you will develop a blood clot, bleeding problems, myelodysplastic syndrome (MDS; a blood disorder that can lead to cancer), or liver disease. Also tell your doctor if you have had surgery to remove your spleen.
  • tell your doctor if you are pregnant, or plan to become pregnant. You should not become pregnant during your treatment with eltrombopag. Use effective birth control while you are receiving treatment and for 7 days after your last dose. If you become pregnant while taking eltrombopag, call your doctor.
  • tell your doctor if you are breastfeeding. You should not breastfeed while you are taking eltrombopag.
  • continue to avoid activities that may cause injury and bleeding during your treatment with eltrombopag. Eltrombopag is given to decrease the risk that you will experience severe bleeding, but there is still a risk that bleeding may occur.

References

  1. https://www.accessdata.fda.gov/drugsatfda_docs/label/2008/022291lbl.pdf
  2. https://www.fda.gov/drugs/postmarket-drug-safety-information-patients-and-providers/promacta-eltrombopag-information
  3. https://www.accessdata.fda.gov/drugsatfda_docs/label/2015/207027s000lbl.pdf
  4. https://www.accessdata.fda.gov/drugsatfda_docs/nda/2008/022291s000_TOC.cfm
  5. https://pubchem.ncbi.nlm.nih.gov/compound/Eltrombopag
  6. https://pubchem.ncbi.nlm.nih.gov/compound/Eltrombopag-olamine
  7. https://go.drugbank.com/salts/DBSALT000063
  8. https://www.cancer.gov/about-cancer/treatment/drugs/eltrombopagolamine
  9. https://en.wikipedia.org/wiki/Eltrombopag
  10. https://medlineplus.gov/druginfo/meds/a609011.html
  11. https://go.drugbank.com/drugs/DB06210
  12. https://www.drugs.com/mtm/eltrombopag.html
  13. https://www.mayoclinic.org/drugs-supplements/eltrombopag-oral-route/side-effects/drg-20072443
  14. NCI Thesaurus Tree
  15. ChemIDplus Chemical Information Classification
  16. CompTox Chemicals Dashboard Chemical Lists
  17. Guide to Pharmacology Target Classification
  18. NORMAN Suspect List Exchange Classification
  19. PubChem