GNH USA

Europe — EMA

Neulasta (Pegfilgrastim)

GNH USA supplies Neulasta (Pegfilgrastim), a myeloid growth factor for preventing chemotherapy‑induced neutropenia and mobilizing stem cells. Request a quote.

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What is Pegfilgrastim?

Pegfilgrastim, the active ingredient in Neulasta, is a granulocyte colony-stimulating factor (G‑CSF) analog presented as a 6 mg/0.6 mL prefilled syringe solution for injection for subcutaneous use. It helps prevent chemotherapy‑induced neutropenia and supports stem cell mobilization in patients undergoing myelosuppressive therapy.

GNH USA supplies Neulasta as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres and pharmacies worldwide.

What is Pegfilgrastim used for?

Neulasta (pegfilgrastim) is a myeloid growth factor used to manage neutrophil deficiency associated with chemotherapy and stem cell collection.

- Chemotherapy‑induced neutropenia: reduces the incidence and duration of severe neutropenia in patients receiving myelosuppressive chemotherapy. - Stem cell mobilization for transplantation: enhances peripheral blood progenitor cell collection in donors prior to autologous or allogeneic stem cell transplantation.

What are the side effects of Pegfilgrastim?

Neulasta may be associated with a range of adverse reactions, which are generally categorized by frequency and severity.

Common Side Effects: - Bone pain: mild to moderate discomfort in bones or joints. - Injection site reactions: redness, swelling or itching at the injection site. - Headache: transient mild headache. - Fatigue: feeling unusually tired.

Serious or Rare Side Effects: - Splenic rupture: rare but potentially life‑threatening. - Anaphylactic reaction: severe allergic response requiring immediate medical attention. - Leukocytosis: excessively high white blood cell count.

What precautions apply to Pegfilgrastim?

Neulasta requires careful clinical consideration before use.

- Assess baseline neutrophil count: verify patient’s absolute neutrophil count before administration. - Avoid concurrent myelosuppressive agents: do not give with other drugs that further suppress bone marrow. - Monitor for bone pain: provide analgesics as needed. - Use caution in patients with splenic disorders: increased risk of splenic complications. - Pregnancy and breastfeeding: safety not established; weigh benefits versus risks. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Pegfilgrastim interact with?

Neulasta can interact with other medicines; some combinations require avoidance while others need monitoring.

Major Interactions (Avoid): - Live vaccines: may increase infection risk; avoid within two weeks of administration. - Other G‑CSF products: additive effects on neutrophil counts; avoid simultaneous use.

Moderate Interactions (Monitor Closely): - Corticosteroids: may reduce efficacy; monitor neutrophil response. - Chemotherapy agents: schedule timing to avoid overlapping peaks; monitor blood counts. - Anticoagulants: rare reports of bleeding; observe for signs of hemorrhage.

Frequently asked questions

What is Neulasta used for?+
Neulasta (pegfilgrastim) is prescribed to reduce the risk of severe neutropenia in patients receiving myelosuppressive chemotherapy and to facilitate the collection of peripheral blood stem cells for autologous or allogeneic transplantation.
How does pegfilgrastim work?+
Pegfilgrastim binds to the granulocyte‑colony stimulating factor receptor on bone‑marrow precursors, activating signaling pathways that stimulate proliferation, differentiation and activation of neutrophil lineage cells, thereby raising the absolute neutrophil count.
What is the usual dose of Neulasta?+
The prescribed dose of Neulasta is determined by the treating physician based on the patient’s chemotherapy regimen and clinical condition. Typically, a single subcutaneous injection is given once per chemotherapy cycle, but exact dosing is individualized.
Is Neulasta safe in pregnancy or breastfeeding?+
Safety data for pegfilgrastim in pregnancy and lactation are limited. The product is classified as pregnancy category unknown, so it should only be used when the potential benefit justifies any potential risk to the fetus or infant.
How do I order Neulasta from GNH USA?+
To place an order, submit an enquiry on the Neulasta product page at gnh-usa.com, specifying the required quantity. GNH USA works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, cold‑chain shipping details and any required import documentation.
How does Neulasta compare with the main alternative drug or class?+
The primary alternative is filgrastim (Neupogen), a non‑pegylated G‑CSF. Pegfilgrastim has a longer half‑life, allowing a single dose per chemotherapy cycle, whereas filgrastim often requires daily injections. Both achieve neutrophil recovery, but pegfilgrastim offers greater convenience at the cost of a higher per‑dose price.
How should Neulasta be stored and handled?+
Neulasta must be stored refrigerated between 2 °C and 8 °C. Keep the prefilled syringe in its original carton, protect it from light, and do not freeze or shake the product. If refrigeration is temporarily unavailable, it may be kept at room temperature for up to 24 hours.
How is Neulasta administered?+
Neulasta is supplied as a prefilled syringe for subcutaneous injection. The injection is given in the abdomen, thigh or upper arm, preferably at least 24 hours after the end of a chemotherapy infusion, following the prescriber’s instructions.
What are the most serious risks to watch for?+
Serious adverse events include splenic rupture, anaphylactic reactions and severe leukocytosis. Patients should be educated to seek immediate medical attention for sudden abdominal pain, signs of an allergic reaction such as difficulty breathing, or unexplained fever and malaise.
Who should not use Neulasta?+
Neulasta is contraindicated in patients with a known hypersensitivity to pegfilgrastim or any of its excipients. Caution is also advised for individuals with a history of splenic disorders, sickle‑cell disease, or uncontrolled active infections.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Pegfilgrastim
Route
Subcutaneous Use
Manufacturer
Amgen Europe B.V.
Origin
EU

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