Product image of Navelbine (Vinorelbine Tartrate) supplied by GNH India

Navelbine

Active Ingredient:
Vinorelbine Tartrate
Origin:
EU

Navelbine (Vinorelbine Tartrate)

Vinorelbine tartrate, the active ingredient in Navelbine, is a Vinca alkaloid presented as a sterile injectable solution for intravenous use. It is employed in the treatment of certain advanced solid tumours, primarily non‑small cell lung cancer and metastatic breast cancer, in adult patients.

GNH India supplies Navelbine as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres worldwide.

Manufacturer / TM Owner

Pierre Fabre Medicament

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Indications & Clinical Uses

  • Vinorelbine is a chemotherapy agent used in the management of solid tumours, particularly within the lung and breast cancer pathways.
  • Non‑small cell lung cancer: helps to inhibit tumour growth and improve disease control in advanced stages.
  • Metastatic breast cancer: used to reduce tumour progression and extend survival.
  • Combination chemotherapy regimens: incorporated to enhance antitumour activity when used with other cytotoxic agents in various solid tumours.

How It Works

  • Vinorelbine binds to tubulin, preventing its polymerisation into microtubules. This inhibition disrupts the formation of the mitotic spindle, arresting cells in the M phase of the cell cycle and ultimately leading to apoptosis of rapidly dividing cancer cells.

Side Effects

Vinorelbine may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects

  • Neutropenia: reduced neutrophil count increasing infection risk.
  • Nausea and vomiting: gastrointestinal upset commonly reported.
  • Constipation: decreased bowel motility.
  • Alopecia: hair loss during treatment.

Serious or Rare Side Effects

  • Severe neutropenia with febrile infection: potentially life‑threatening.
  • Hypersensitivity reactions: including rash, bronchospasm, or anaphylaxis.
  • Pulmonary toxicity: interstitial pneumonitis or fibrosis.
  • Peripheral neuropathy: nerve damage causing tingling or pain.
  • Cardiac arrhythmias: irregular heart rhythms requiring monitoring.

Precautions & Warnings

  • Vinorelbine requires careful monitoring and specific safety measures before and during therapy.
  • Monitor blood counts: perform regular complete blood counts to detect myelosuppression.
  • Assess liver function: evaluate hepatic enzymes as the drug is metabolised hepatically.
  • Evaluate pulmonary status: use caution in patients with pre‑existing lung disease.
  • Avoid in severe renal impairment: dose adjustment may be necessary.
  • Use with caution when combined with other myelosuppressive agents.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Vinorelbine can interact with several drug classes, necessitating vigilance.

Major Interactions (Avoid)

  • Concurrent myelosuppressive chemotherapy: may exacerbate bone‑marrow suppression.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): increase vinorelbine plasma levels.
  • Live vaccines: risk of infection due to immunosuppression.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce efficacy.
  • Anticoagulants (e.g., warfarin): monitor coagulation parameters for bleeding risk.

Frequently Asked Questions

Navelbine is a chemotherapy medication indicated for the treatment of advanced non‑small cell lung cancer and metastatic breast cancer. It is administered intravenously and works as part of a broader oncologic regimen to control tumour growth and improve patient outcomes.

Vinorelbine interferes with microtubule assembly by binding to tubulin, which prevents the formation of the mitotic spindle. This halts cell division during the M phase, leading to apoptosis of rapidly proliferating cancer cells.

The specific dose of Navelbine is determined by the prescribing oncologist based on the patient’s condition, body surface area, and treatment protocol. Dosing regimens are individualized and should follow the clinician’s instructions.

Vinorelbine is classified as contraindicated in pregnancy because it may cause fetal harm. It is also not recommended during breastfeeding, as it can be excreted in milk and affect the infant. Women of child‑bearing potential should use effective contraception.

To order Navelbine, 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, shipping details (including cold‑chain if needed), and import documentation.

Compared with other Vinca alkaloids such as vincristine, vinorelbine has a distinct toxicity profile, showing less neurotoxicity but a higher incidence of myelosuppression. Its efficacy in NSCLC and breast cancer is well‑established, making it a preferred option in many combination regimens.

Navelbine should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen or shaken. Keep the vial in its original packaging until use to maintain stability.

Navelbine is given as an intravenous infusion, typically over 6–10 minutes, under the supervision of qualified healthcare professionals. The infusion rate and dilution are determined by the prescribing physician and institutional protocols.

The most serious risks include severe neutropenia leading to infection, hypersensitivity reactions that can be life‑threatening, pulmonary toxicity such as interstitial pneumonitis, and cardiac arrhythmias. Patients should be monitored closely for these events throughout treatment.

Navelbine is contraindicated in patients with known hypersensitivity to vinorelbine or any component of the formulation, in those with severe bone‑marrow suppression, and in pregnant women. Caution is advised for individuals with significant liver or kidney impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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