Product image of Neulasta (Pegfilgrastim) supplied by GNH India

Neulasta

Active Ingredient:
Pegfilgrastim
Origin:
EU

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

Manufacturer / TM Owner

Amgen Europe B.V.

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Indications & Clinical Uses

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.

How It Works

  • Pegfilgrastim is a recombinant pegylated form of granulocyte colony‑stimulating factor. After subcutaneous injection it binds with high affinity to the G‑CSF receptor on neutrophil precursors in the bone marrow, activating intracellular JAK/STAT signaling. This stimulates proliferation, differentiation and activation of neutrophil lineage cells, leading to an increased absolute neutrophil count and accelerated recovery from chemotherapy‑induced myelosuppression.

Side Effects

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.

Precautions & Warnings

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.

Avoid Interactions

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

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.

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.

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.

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.

To place an order, submit an enquiry on the Neulasta product page at gnhindia.com, specifying the required quantity. GNH India 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.

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.

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.

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.

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.

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.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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