promacta eltrombopag olamine 25 mg
1 INDICATIONS AND USAGE PROMACTA is a thrombopoietin receptor agonist indicated: for the treatment of thrombocytopenia in adult and pediatric patients 1 year and older with persistent or chronic immune thrombocytopenia (ITP) who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy. PROMACTA should be used only in patients with ITP whose degree of thrombocytopenia and clinical condition increase the risk for bleeding. ( 1.1 ) for the treatment of thrombocytopenia in patients with chronic hepatitis C to allow the initiation and maintenance of interferon-based therapy. 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. ( 1.2 ) in combination with standard immunosuppressive therapy for the first-line treatment of adult and pediatric patients 2 years and older with severe aplastic anemia. ( 1.3 ) for the treatment of patients with severe aplastic anemia who have had an insufficient response to immunosuppressive therapy. ( 1.3 ) Limitations of Use: PROMACTA is not indicated for the treatment of patients with myelodysplastic syndrome (MDS). ( 1.4 ) Safety and efficacy have not been established in combination with direct-acting antiviral agents used without interferon for treatment of chronic hepatitis C infection. ( 1.4 ) 1.1 Treatment of Thrombocytopenia in Patients With Persistent or Chronic Immune Thrombocytopenia PROMACTA is indicated for the treatment of thrombocytopenia in adult and pediatric patients 1 year and older with persistent or chronic immune thrombocytopenia (ITP) who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy. PROMACTA should be used only in patients with ITP whose degree of thrombocytopenia and clinical condition increase the risk for bleeding. 1.2 Treatment of Thrombocytopenia in Patients With Hepatitis C Infection PROMACTA is indicated for the treatment of thrombocytopenia in patients with chronic hepatitis C to allow the initiation and maintenance of interferon-based therapy. 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. 1.3 Treatment of Severe Aplastic Anemia PROMACTA is indicated in combination with standard immunosuppressive therapy (IST) for the first-line treatment of adult and pediatric patients 2 years and older with severe aplastic anemia. PROMACTA is indicated for the treatment of patients with severe aplastic anemia who have had an insufficient response to immunosuppressive therapy. 1.4 Limitations of Use PROMACTA is not indicated for the treatment of patients with myelodysplastic syndromes (MDS) [see Warnings and Precautions (5.3)] . Safety and efficacy have not been established in combination with direct-acting antiviral agents used without interferon for treatment of chronic hepatitis C infection.
novartis pharmaceuticals corporation
ROUND ORANGE GS NX3 25
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promacta eltrombopag olamine 50 mg
novartis pharmaceuticals corporation
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16 HOW SUPPLIED/STORAGE AND HANDLING 16.1 Tablets The 12.5-mg tablets are round, biconvex, white, film-coated tablets debossed with “GS MZ1” and 12.5 on one side and are available in bottles of 30: NDC 0078-0684-15 The 25-mg tablets are round, biconvex, orange, film-coated tablets debossed with “GS NX3” and 25 on one side and are available in bottles of 30: NDC 0078-0685-15 The 50-mg tablets are round, biconvex, blue, film-coated tablets debossed with “GS UFU” and 50 on one side and are available: Bottles of 14 NDC 0078-0686-55 Bottles of 30 NDC 0078-0686-15 The 75-mg tablets are round, biconvex, pink, film-coated tablets debossed with “GS FFS” and 75 on one side and are available in bottles of 30: NDC 0078-0687-15 Store at room temperature between 20°C to 25°C (68°F to 77°F); excursions permitted between 15°C and 30°C (59°F and 86°F) [see USP Controlled Room Temperature]. Dispense in original bottle. 16.2 For Oral Suspension The 12.5-mg for oral suspension is a reddish-brown to yellow powder in unit-dose packets, copackaged in a kit with a 40-cc reconstitution vessel, a threaded closure with syringe-port capability, and 30 single-use oral dosing syringes. Each kit (NDC 0078-0972-61) contains 30 packets: NDC 0078-0972-19 The 25-mg for oral suspension is a reddish-brown to yellow powder in unit-dose packets, copackaged in a kit with a 40-cc reconstitution vessel, a threaded closure with syringe-port capability, and 30 single-use oral dosing syringes. Each kit (NDC 0078-0697-61) contains 30 packets: NDC 0078-0697-19 Store at room temperature between 20°C to 25°C (68°F to 77°F); excursions permitted between 15°C and 30°C (59°F and 86°F) [see USP Controlled Room Temperature]. Following reconstitution, the product should be administered immediately but may be stored for a maximum period of 30 minutes between 20°C to 25°C (68°F to 77°F); excursions permitted between 15°C and 30°C (59°F and 86°F) [see USP Controlled Room Temperature]. Throw away (discard) the mixture if not used within 30 minutes.
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