Product image of Neupogen Singleject (Filgrastim) supplied by GNH India

Neupogen Singleject

Active Ingredient:
Filgrastim
Origin:
EU

Neupogen Singleject (Filgrastim)

Filgrastim, the active ingredient in Neupogen Singleject, is a granulocyte colony-stimulating factor presented as a 300 µg/0.5 mL solution for injection (prefilled syringe) for intravenous or subcutaneous use. It treats neutropenia associated with chemotherapy and other hematologic conditions in patients requiring neutrophil support.

GNH India supplies Neupogen Singleject as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Amgen Europe B.V.

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Indications & Clinical Uses

Neupogen Singleject (filgrastim) is used to stimulate neutrophil production in a range of hematologic disorders.

  • Neutropenia associated with chemotherapy: restores neutrophil counts to reduce infection risk.
  • Aplastic anemia: supports bone‑marrow recovery by promoting neutrophil lineage development.
  • Peripheral blood stem cell mobilization: enhances stem‑cell yield for collection prior to transplantation.
  • Myelodysplastic syndromes: improves neutrophil numbers in patients with ineffective hematopoiesis.
  • Severe chronic neutropenia: provides long‑term neutrophil support to lower infection susceptibility.

How It Works

  • Filgrastim binds to the specific G‑CSF receptor on hematopoietic progenitor cells in the bone marrow, activating intracellular signaling pathways that drive proliferation, differentiation, and activation of neutrophil precursors. This results in increased production and release of mature neutrophils into the peripheral blood, thereby raising the absolute neutrophil count.

Side Effects

Filgrastim may cause a range of adverse reactions, from mild to serious.

Common Side Effects

  • Bone pain: discomfort in the limbs or back, often related to rapid marrow expansion.
  • Injection site reactions: redness, swelling, or mild tenderness at the injection site.
  • Headache: transient mild to moderate headache.
  • Fatigue: general feeling of tiredness.
  • Fever: low‑grade temperature elevation.
  • Nausea: mild gastrointestinal upset.

Serious or Rare Side Effects

  • Splenic rupture: sudden abdominal pain and signs of internal bleeding.
  • Acute respiratory distress syndrome (ARDS): severe breathing difficulty requiring urgent care.
  • Severe allergic reactions: rash, itching, swelling, or anaphylaxis.
  • Leukocytosis: excessively high white‑blood‑cell counts.
  • Capillary leak syndrome: sudden fluid shift leading to edema and low blood pressure.
  • Severe bone pain: intense, persistent pain requiring medical intervention.

Precautions & Warnings

When using Neupogen Singleject, clinicians should observe several safety measures.

  • Monitor blood counts: check neutrophil levels regularly to assess response.
  • Assess for splenomegaly: perform abdominal examinations before and during therapy.
  • Avoid in patients with known hypersensitivity: do not administer if allergic to filgrastim or excipients.
  • Use caution in sickle‑cell disease: monitor for vaso‑occlusive crises.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Filgrastim may interact with other medications, requiring attention to potential effects.

Major Interactions (Avoid)

  • Concurrent use of other colony‑stimulating factors: risk of excessive leukocytosis.
  • Monoclonal antibodies targeting G‑CSF: may antagonize filgrastim activity.
  • High‑dose systemic corticosteroids: can blunt neutrophil response.

Moderate Interactions (Monitor Closely)

  • Cytotoxic chemotherapy agents: may mask myelosuppression if filgrastim timing is altered.
  • Live vaccines: reduced efficacy; consider timing relative to filgrastim administration.
  • Anticoagulants: increased risk of bleeding at injection sites.
  • Certain antibiotics: may affect infection‑risk assessment during neutropenia treatment.

Frequently Asked Questions

Neupogen Singleject contains filgrastim, a granulocyte colony‑stimulating factor that is prescribed to increase neutrophil counts in patients with chemotherapy‑induced neutropenia, aplastic anemia, severe chronic neutropenia, myelodysplastic syndromes, and for peripheral blood stem‑cell mobilization prior to transplantation.

Filgrastim binds to the G‑CSF receptor on bone‑marrow progenitor cells, activating signaling pathways that stimulate the proliferation, differentiation, and maturation of neutrophil precursors. This leads to a rapid rise in circulating neutrophils, helping the immune system fight infections.

The exact dose and schedule of Neupogen Singleject are determined by the prescribing clinician based on the patient’s condition, weight, and treatment protocol. The product is supplied as a 300 µg/0.5 mL prefilled syringe for intravenous or subcutaneous administration.

The safety of filgrastim in pregnancy and lactation has not been fully established. It should only be used if the potential benefit justifies any potential risk to the fetus or infant, and the decision must be made by the treating physician.

To place an order, submit an enquiry on the 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 necessary import documentation.

Neupogen Singleject (filgrastim) is a recombinant form of human G‑CSF, similar in efficacy to other filgrastim products and biosimilars. Compared with pegylated G‑CSF (pegfilgrastim), filgrastim typically requires daily dosing, whereas pegfilgrastim is given once per chemotherapy cycle, but both achieve comparable neutrophil recovery.

Neupogen Singleject must be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Before use, the prefilled syringe can be allowed to reach room temperature for a few minutes, but the product should be used promptly after removal from refrigeration.

The medication is supplied in a prefilled syringe and can be given either intravenously or subcutaneously, as directed by the prescriber. The injection site should be rotated for subcutaneous administration, and aseptic technique must be observed for all routes.

Serious adverse events include splenic rupture, acute respiratory distress syndrome, severe allergic reactions (anaphylaxis), capillary leak syndrome, and uncontrolled leukocytosis. Patients should be monitored for abdominal pain, respiratory difficulty, rash, or sudden swelling, and any concerning symptoms should prompt immediate medical evaluation.

Neupogen Singleject is contraindicated in individuals with known hypersensitivity to filgrastim or any of its excipients. It should also be used with caution in patients with sickle‑cell disease, underlying splenomegaly, or those receiving other colony‑stimulating factors, and only under close medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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