Nivestym Generic Name & Formulations
Legal Class
Rx
General Description
Filgrastim-aafi 300mcg, 480mcg; soln for SC inj or IV infusion; preservative-free.
Pharmacological Class
Granulocyte colony stimulating factor.
How Supplied
Prefilled syringes (0.5mL, 0.8mL)—1, 10; Vials (1mL, 1.6mL)—10
Manufacturer
Generic Availability
NO
Mechanism of Action
Colony-stimulating factors are glycoproteins which act on hematopoietic cells by binding to specific cell surface receptors and stimulating proliferation‚ differentiation commitment‚ and some end-cell functional activation.
Nivestym Indications
Indications
See full labeling. To decrease incidence of infection in patients with nonmyeloid malignancies receiving certain myelosuppressive anti-cancer drugs. To reduce time to neutrophil recovery and fever duration after induction or consolidation chemotherapy treatment of adults with AML. To reduce duration of neutropenia and related sequelae in patients with nonmyeloid malignancies undergoing myeloablative chemotherapy followed by bone-marrow transplantation (BMT). To mobilize hematopoietic progenitor cells (PBPC) into peripheral blood for collection by leukapheresis. To reduce the incidence and duration of neutropenia sequelae in severe chronic neutropenia (SCN).
Nivestym Dosage and Administration
Adult
See full labeling. Do not give for ≥24hrs before or after cytotoxic chemotherapy dose. BMT: Give 1st dose ≥24hrs after bone marrow infusion. PBPC mobilization: Give ≥4 days before first leukapheresis and continue until the last leukapheresis. SCN: Give on a daily basis.
Children
See full labeling.
Nivestym Contraindications
Not Applicable
Nivestym Boxed Warnings
Not Applicable
Nivestym Warnings/Precautions
Warnings/Precautions
Monitor blood, including CBC and differential and platelets, before and during therapy (myelosuppressive chemotherapy: monitor twice weekly; BMT: monitor frequently following transplantation; SCN: monitor during initial 4 weeks of therapy and during 2 weeks after dose adjustment, then monthly once clinically stable). Discontinue if post nadir absolute neutrophil count (ANC) >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 develops. Confirm diagnosis and do appropriate pretreatment hematological workup in SCN. Sickle cell disease: may cause severe sickle cell crisis (discontinue if occurs). Consider reducing or interrupting dose if glomerulonephritis suspected. Monitor for MDS/AML in those with severe chronic neutropenia, breast or lung cancer. Monitor for aortitis; discontinue if suspected. Avoid simultaneous chemo- and radiation therapy. Withhold therapy if cutaneous vasculitis occurs; resume at lower dose when resolved. Permanently discontinue if serious allergic reactions occur. PBPC mobilization: not for use in healthy donors. Possible transient (+) bone imaging changes in nuclear imaging. Pregnancy. Nursing mothers.
Nivestym Pharmacokinetics
Distribution
Averaged volume of distribution: 150 mL/kg.
Elimination
Half-life: ~3.5 hours.
Nivestym Interactions
Not Applicable
Nivestym Adverse Reactions
Adverse Reactions
Pyrexia, pain, rash, cough, dyspnea, epistaxis, bone pain, headache, anemia, diarrhea, hypoesthesia, alopecia; thrombocytopenia, cutaneous vasculitis, splenomegaly, ARDS, capillary leak syndrome (monitor), others (see full labeling).
Nivestym Clinical Trials
See Literature
Nivestym Note
Not Applicable
Nivestym Patient Counseling
See Literature