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Granocyte

Active Ingredient:
Lenograstim
Origin:
EU

Granocyte (Lenograstim)

Granocyte is an injectable solution containing the recombinant granulocyte colony‑stimulating factor lenograstim. It is supplied in a standard concentration for intravenous or subcutaneous administration and is marketed in the European Union as a prescription‑only hematopoietic growth factor. The product is used to support neutrophil recovery in patients undergoing chemotherapy, bone‑marrow transplantation, or stem‑cell mobilization, and it is classified under ATC code L03AA02 as part of standard supportive care protocols.

Manufacturer / TM Owner

Sanofi-Aventis Monoprosopi A.E.B.E

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Indications & Clinical Uses

Granocyte is indicated for several hematologic conditions where neutrophil counts are compromised.

  • Management of chemotherapy‑induced neutropenia to reduce infection risk.
  • Treatment of neutropenia following allogeneic or autologous bone‑marrow transplantation.
  • Mobilization of peripheral blood stem cells for collection prior to transplantation.
  • Support of neutrophil recovery in patients receiving high‑dose radiation therapy.

Side Effects

Adverse reactions to lenograstim are generally mild to moderate, but serious events can occur.

Common

  • Bone pain, especially in the lower back or hips.
  • Mild fever or flu‑like symptoms.
  • Injection site erythema or discomfort.
  • Nausea or mild gastrointestinal upset.

Serious

  • Splenic rupture or enlargement.
  • Acute respiratory distress syndrome (ARDS).
  • Severe allergic reactions such as anaphylaxis.
  • Capillary leak syndrome.

Precautions & Warnings

When prescribing Granocyte, clinicians should evaluate patient history and monitor for specific safety concerns.

  • Assess baseline neutrophil counts and overall bone‑marrow function before initiation.
  • Use caution in patients with a history of splenic disorders or abdominal trauma.
  • Avoid in individuals with known hypersensitivity to lenograstim or any excipients.
  • Monitor for signs of infection, fever, or unexpected inflammation during therapy.
  • Consider dose adjustment or discontinuation if severe bone pain or systemic reactions develop.
  • Pregnancy and lactation status should be reviewed, as safety data are limited.

Avoid Interactions

Lenograstim may interact with other medications or clinical conditions that affect immune function or hematopoiesis.

Avoid

  • Concurrent use of other granulocyte colony‑stimulating factors or high‑dose corticosteroids without specialist guidance.
  • Live vaccines administered during treatment, due to altered immune response.

Use with caution

  • Chemotherapeutic agents that cause profound myelosuppression, requiring close monitoring of blood counts.
  • Anticoagulants, as changes in platelet function may occur.
  • Immunosuppressive biologics, which could modify the efficacy of neutrophil recovery.

Frequently Asked Questions

Granocyte is a prescription‑only injectable solution whose active ingredient is the recombinant protein lenograstim, a granulocyte colony‑stimulating factor.

It is commonly prescribed for patients who develop neutropenia after chemotherapy, those undergoing bone‑marrow transplantation, and individuals requiring peripheral blood stem‑cell mobilization.

Lenograstim binds to the G‑CSF receptor on hematopoietic progenitor cells, stimulating their proliferation, differentiation, and activation into mature neutrophils.

Yes, the injectable solution is approved for administration by either intravenous infusion or subcutaneous injection, depending on clinical need.

Common adverse effects include bone pain, mild fever or flu‑like symptoms, injection‑site redness or discomfort, and occasional nausea or mild gastrointestinal upset.

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

Patients with a history of splenic disorders, recent abdominal trauma, or known hypersensitivity to lenograstim or its excipients should be evaluated carefully before treatment.

Live vaccines are generally avoided during Granocyte therapy because the altered immune response may affect vaccine efficacy and safety.

Concurrent use of additional granulocyte colony‑stimulating factors or high‑dose corticosteroids is discouraged unless directed by a specialist, due to potential overlapping effects.

Regular blood counts to assess neutrophil recovery, evaluation for signs of infection or fever, and observation for bone pain or unexpected systemic reactions are recommended.

Safety data for lenograstim in pregnancy and lactation are limited; the pregnancy category is listed as unknown, so risk‑benefit assessment is required.

Granocyte is classified under the Anatomical Therapeutic Chemical (ATC) code L03AA02, which denotes granulocyte colony‑stimulating factors.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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