Releuko Generic Name & Formulations
Legal Class
General Description
Pharmacological Class
How Supplied
Prefilled syringes (0.5mL, 0.8mL)—1, 10; Vials (1mL, 1.6mL)—10
Manufacturer
Generic Availability
Mechanism of Action
Releuko Indications
Indications
Releuko Dosage and Administration
Adult
Children
Releuko Contraindications
Not Applicable
Releuko Boxed Warnings
Not Applicable
Releuko Warnings/Precautions
Warnings/Precautions
Monitor blood, including CBCs, differentials, and platelets, before and during therapy (myelosuppressive chemotherapy: monitor twice weekly; BMT: frequently after transplant; SCN: during initial 4 weeks of therapy and during 2 weeks after dose adjustment). Discontinue if post nadir absolute neutrophil count (ANC) reaches >10,000/mm3 for patients receiving myelosuppressive chemotherapy; other indications: see full labeling. Monitor for splenomegaly/splenic rupture and for acute respiratory distress syndrome (ARDS); discontinue if ARDS occurs. Confirm diagnosis and do appropriate pretreatment hematological workup in SCN. Sickle cell disease: may cause severe sickle cell crisis (discontinue if occurs). Glomerulonephritis. Monitor for MDS/AML in those with severe chronic neutropenia, breast or lung cancer. Monitor for aortitis; discontinue if suspected. Avoid simultaneous use with chemo and radiation therapy. Permanently discontinue if serious allergic reactions occur. Possible transient (+) bone imaging changes in nuclear imaging. Pregnancy. Nursing mothers.
Releuko Pharmacokinetics
Distribution
Volume of distribution: 150 mL/kg (after IV administration).
Elimination
Half-life: ~3.5 hours (after IV administration).
Releuko Interactions
Not Applicable
Releuko Adverse Reactions
Adverse Reactions
Releuko Clinical Trials
See Literature
Releuko Note
Not Applicable
Releuko Patient Counseling
See Literature
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