Europe — EMA
Neulasta (Pegfilgrastim)
GNH USA supplies Neulasta (Pegfilgrastim), a granulocyte colony‑stimulating factor for chemotherapy‑induced neutropenia and stem‑cell mobilization.
Request sourcing
What is Pegfilgrastim?
Pegfilgrastim, the active ingredient in Neulasta, is a Granulocyte colony‑stimulating factor (G‑CSF) presented as a 6 mg injection (prefilled syringe) for subcutaneous use. It reduces the duration of chemotherapy‑induced neutropenia and assists in mobilizing peripheral blood stem cells for collection.
GNH USA supplies Neulasta as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.
What is Pegfilgrastim used for?
Neulasta (pegfilgrastim) is a granulocyte colony‑stimulating factor used to support patients undergoing myelosuppressive chemotherapy.
- Chemotherapy‑induced neutropenia: reduces the duration and severity of neutropenia in patients receiving myelosuppressive chemotherapy. - Peripheral blood stem cell mobilization: facilitates collection of stem cells for autologous transplantation. - Hematopoietic recovery after high‑dose chemotherapy: accelerates neutrophil recovery to lower infection risk.
What are the side effects of Pegfilgrastim?
Common Side Effects: - Bone pain: mild to moderate discomfort often reported after injection. - Injection site reactions: redness, swelling, or tenderness at the administration site. - Fatigue: transient feeling of tiredness. - Nausea: occasional upset stomach. - Headache: mild headache may occur.
Serious or Rare Side Effects: - Severe allergic reactions: anaphylaxis, angioedema, or rash requiring immediate medical attention. - Splenic rupture: rare but potentially life‑threatening abdominal emergency. - Acute respiratory distress syndrome (ARDS): severe breathing difficulty. - Capillary leak syndrome: sudden drop in blood pressure and fluid accumulation. - Leukocytosis: excessively high white blood cell counts.
What precautions apply to Pegfilgrastim?
Neulasta should be used under close medical supervision with attention to patient‑specific factors.
- Dose adjustment: follow prescriber instructions based on chemotherapy regimen and patient characteristics. - Renal impairment: monitor patients with severe renal dysfunction, as clearance may be altered. - Bone pain management: assess and treat pain proactively, especially after the first dose. - Allergic reactions: discontinue immediately if signs of hypersensitivity appear. - Concomitant myeloid growth factors: avoid simultaneous use to prevent overlapping effects. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.
What does Pegfilgrastim interact with?
Pegfilgrastim may interact with other agents that affect bone marrow or immune function.
Major Interactions (Avoid): - Concurrent use with other myeloid growth factors: may increase risk of bone marrow suppression. - Live vaccines: may reduce vaccine efficacy; avoid administration during treatment.
Moderate Interactions (Monitor Closely): - Cytotoxic chemotherapy: timing must be coordinated to avoid reduced chemotherapy efficacy. - Antibiotics that affect neutrophil function: monitor blood counts for additive effects. - Corticosteroids: may mask signs of infection; observe patients closely.
Frequently asked questions
What is Neulasta used for?+
How does pegfilgrastim work?+
What is the usual dose of Neulasta?+
Is Neulasta safe in pregnancy or breastfeeding?+
How do I order Neulasta from GNH USA?+
How does Neulasta compare with the main alternative drug?+
What are the storage and handling requirements for Neulasta?+
How is Neulasta administered?+
What are the most serious risks associated with Neulasta?+
Who should not use Neulasta?+
Product details
Related products

Neulasta 10 mg
Pegfilgrastim · 10 MG

Lapelga 6 mg
Pegfilgrastim · 6 MG

Fulphila 10 mg
Pegfilgrastim · 10 MG

Ziextenzo 6 mg
Pegfilgrastim · 6 MG