Product image of Granulokine (Filgrastim) supplied by GNH India

Granulokine

Active Ingredient:
Filgrastim
Origin:
EU

Granulokine (Filgrastim)

Granulokine is a prescription medication containing the active ingredient filgrastim, supplied in an injectable form for intravenous or subcutaneous administration. It is classified as a granulocyte colony‑stimulating factor (G‑CSF) and is marketed in the European Union. The product is used to stimulate neutrophil production in patients with certain hematologic conditions. It is available only by prescription and is not an over‑the‑counter product in most EU countries.

Manufacturer / TM Owner

Amgen Europe B.V.

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Indications & Clinical Uses

Granulokine is indicated for several clinical situations in which neutrophil counts are low or need to be increased.

  • Chemotherapy‑induced neutropenia to reduce the risk of infection.
  • Aplastic anemia to support bone‑marrow recovery.
  • Mobilization of peripheral blood progenitor cells for stem‑cell collection.
  • Preparation for bone‑marrow transplantation to improve engraftment.
  • Treatment of severe chronic neutropenia when other therapies are insufficient.

Side Effects

The safety profile of Granulokine includes both frequently observed reactions and less common but potentially serious events.

Common

  • Bone pain, especially in the hips, sternum or long bones.
  • Mild fever or chills.
  • Headache or dizziness.
  • Injection‑site erythema or swelling.

Serious

  • Splenic rupture or enlargement.
  • Acute respiratory distress syndrome.
  • Severe allergic reactions such as anaphylaxis.

Precautions & Warnings

The clinician should evaluate several precautionary factors before initiating Granulokine therapy to minimize risk.

  • Assess baseline neutrophil count and overall bone‑marrow function.
  • Use caution in patients with a history of splenic disorders or abdominal trauma.
  • Monitor for signs of hypersensitivity during and after administration.
  • Adjust dosing in patients with renal impairment as recommended by prescribing information.
  • Avoid use in individuals with known hypersensitivity to filgrastim or any excipients.
  • Consider pregnancy and lactation status; data are limited, so weigh potential benefits against unknown risks.

Avoid Interactions

Granulokine may interact with other medications, affecting its efficacy or safety profile.

Avoid

  • Concurrent use with chemotherapy agents that cause profound myelosuppression without appropriate timing.
  • Combination with other colony‑stimulating factors (e.g., sargramostim) unless specifically directed.

Use with caution

  • Antimicrobial agents such as penicillins that may mask infection signs.
  • Corticosteroids, which can alter neutrophil dynamics.
  • Immunosuppressive drugs that could modify the expected rise in neutrophil counts.

Frequently Asked Questions

Granulokine contains filgrastim, a recombinant granulocyte colony‑stimulating factor that binds to G‑CSF receptors on hematopoietic progenitor cells, stimulating proliferation, differentiation and activation of neutrophil precursors, which raises circulating neutrophil counts.

Granulokine is prescribed for patients who have chemotherapy‑induced neutropenia, aplastic anemia, are undergoing bone‑marrow transplantation, need peripheral blood progenitor cell mobilization, or have severe chronic neutropenia unresponsive to other treatments.

The medication is supplied as an injectable solution and can be given either intravenously or subcutaneously, according to the prescribing information and clinical situation.

Common adverse reactions include bone pain, mild fever or chills, headache or dizziness, and localized injection‑site erythema or swelling.

Serious events, although rare, may include splenic rupture or enlargement, acute respiratory distress syndrome, and severe allergic reactions such as anaphylaxis.

Dose adjustment may be required for patients with renal impairment; clinicians should follow the specific dosing recommendations provided in the product label.

Pregnancy safety data are limited; the drug should only be used if the potential benefit justifies the potential risk to the fetus.

Concurrent use with other G‑CSFs such as sargramostim is generally avoided unless specifically directed by a specialist, to prevent overlapping effects.

Regular blood counts to assess neutrophil response, monitoring for signs of splenic enlargement, and observation for any allergic reactions are recommended during therapy.

Some antibiotics, particularly penicillins, may mask infection signs; they can be used with caution, ensuring that clinicians remain vigilant for underlying infections.

Severe bone pain should be reported to the prescribing physician; analgesics may be considered, and the treatment plan may be reassessed.

No, Granulokine is a prescription‑only medication and must be prescribed by a qualified healthcare professional.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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