Nyvepria

— THERAPEUTIC CATEGORIES —
  • White blood cell disorders

Nyvepria Generic Name & Formulations

General Description

Pegfilgrastim-apgf 6mg/0.6mL; soln for SC inj; preservative-free.

Pharmacological Class

Granulocyte colony stimulating factor.

How Supplied

Single-dose prefilled syringe—1 (w. supplies)

Manufacturer

Generic Availability

NO

Nyvepria Indications

Indications

To decrease the incidence of infection, as manifested by febrile neutropenia, in patients with non-myeloid malignancies receiving myelosuppressive anticancer drugs associated with a clinically significant incidence of febrile neutropenia.

Limitations of Use

Not for the mobilization of peripheral blood progenitor cells for hematopoietic stem cell transplantation.

Nyvepria Dosage and Administration

Adults and Children

See full labeling. ≥45kg: Do not give between 14 days before and 24 hours after chemotherapy. 6mg SC once per chemotherapy cycle. Children (<10kg): 0.1mg/kg; (10–20kg): 1.5mg; (21–30kg): 2.5mg; (31–44kg): 4mg. Direct administration of prefilled syringe with doses <6mg is not recommended.

Nyvepria Contraindications

Not Applicable

Nyvepria Boxed Warnings

Not Applicable

Nyvepria Warnings/Precautions

Warnings/Precautions

Monitor for splenomegaly, splenic rupture, acute respiratory distress syndrome (ARDS); evaluate if fever, lung infiltrates, or respiratory distress occurs; discontinue if ARDS diagnosed. Permanently discontinue if serious allergic reactions develop. Sickle cell disorders; discontinue if sickle cell crisis occurs. Monitor for glomerulonephritis; consider dose reduction or interruption if treatment-related. Monitor CBC, platelet counts during therapy. Discontinue if aortitis is suspected. Myeloid malignancies. Myelodysplasia. Monitor for MDS/AML in those with breast or lung cancer. Possible transient (+) bone imaging changes in nuclear imaging. Pregnancy. Nursing mothers.

Nyvepria Pharmacokinetics

See Literature

Nyvepria Interactions

Not Applicable

Nyvepria Adverse Reactions

Adverse Reactions

Bone or extremity pain; anaphylaxis, ARDS, splenic rupture, glomerulonephritis, leukocytosis, aortitis, capillary leak syndrome (monitor closely if occurs), thrombocytopenia.

Nyvepria Clinical Trials

See Literature

Nyvepria Note

Not Applicable

Nyvepria Patient Counseling

See Literature