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

Navelbine

Active Ingredient:
Vinorelbine Tartrate
Origin:
EU

Navelbine (Vinorelbine Tartrate)

Vinorelbine, the active ingredient in Navelbine, is a Vinca alkaloid presented as an intravenous solution for intravenous use. It is employed in the treatment of certain solid tumours, notably non‑small cell lung cancer and metastatic breast cancer, and is administered under the supervision of oncology specialists.

GNH India supplies Navelbine as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide, ensuring quality and regulatory compliance while providing reliable global distribution.

Manufacturer / TM Owner

Pierre Fabre Pharma S.R.L.

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Indications & Clinical Uses

Vinorelbine is a Vinca alkaloid used in chemotherapy for solid tumours.

  • Non‑small cell lung cancer: improves disease control and may extend survival in patients with advanced disease.
  • Metastatic breast cancer: used after failure of anthracycline‑based therapy to reduce tumour burden.
  • Solid tumours (in combination regimens): contributes to cytotoxic activity when combined with other chemotherapeutic agents.

How It Works

  • Vinorelbine binds to the tubulin protein within cells, inhibiting microtubule polymerisation. This disruption prevents the formation of a functional mitotic spindle, arresting cell division in the M phase and leading to apoptosis of rapidly proliferating cancer cells.

Side Effects

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

Common Side Effects

  • Neutropenia: reduced white blood cell count increasing infection risk.
  • Nausea and vomiting: gastrointestinal upset common during treatment.
  • Fatigue: persistent tiredness affecting daily activities.
  • Alopecia: hair loss that may be temporary.

Serious or Rare Side Effects

  • Severe neutropenia with fever: requires immediate medical attention.
  • Pulmonary toxicity: cough, dyspnoea, or interstitial pneumonitis.
  • Hypersensitivity reactions: rash, flushing, or anaphylaxis.
  • Peripheral neuropathy: tingling or numbness in extremities.
  • Cardiac toxicity: arrhythmias or decreased cardiac function.

Precautions & Warnings

Before initiating therapy, clinicians should assess patient-specific risk factors and monitor for toxicity.

  • Monitor blood counts: perform regular CBC to detect neutropenia and thrombocytopenia.
  • Assess liver function: adjust therapy if hepatic impairment is present.
  • Evaluate pulmonary status: baseline and periodic lung function tests are recommended.
  • Use antiemetics prophylactically: to mitigate nausea and vomiting.
  • Store at ambient temperature: keep in original container, protect from light and moisture.

Avoid Interactions

Vinorelbine may interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole): increase vinorelbine exposure and toxicity.
  • Concurrent myelosuppressive agents: exacerbate bone‑marrow suppression.
  • Radiotherapy to the chest: may heighten risk of pulmonary toxicity.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin): reduce vinorelbine plasma levels.
  • Anticoagulants (e.g., warfarin): may increase bleeding tendency.
  • Other anti‑emetics (e.g., ondansetron): can affect drug metabolism.
  • Herbal supplements (e.g., St John's wort): may alter vinorelbine clearance.

Frequently Asked Questions

Navelbine, containing vinorelbine, is indicated for the treatment of non‑small cell lung cancer and metastatic breast cancer. It is administered as part of a chemotherapy regimen under the direction of an oncologist to help control tumour growth and improve patient outcomes.

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

The specific dose of Navelbine is determined by the prescribing oncologist based on factors such as cancer type, disease stage, patient weight, and overall health. Dosage regimens are individualized and should follow the clinician’s instructions.

Vinorelbine is classified as contraindicated in pregnancy because it may cause fetal harm. Women of child‑bearing potential should use effective contraception. Safety during breastfeeding has not been established, and nursing is generally discouraged while receiving treatment.

To request 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 any cold‑chain requirements) and necessary import documentation.

Vinorelbine belongs to the Vinca alkaloid class, which differs from taxanes or anthracyclines in its mechanism of tubulin inhibition. Compared with other agents, vinorelbine often has a distinct toxicity profile, with notable neutropenia but relatively lower cardiac toxicity than anthracyclines.

Navelbine should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the solution from light, moisture and extreme temperature fluctuations to maintain stability.

Navelbine is supplied as an intravenous solution and is given by slow infusion into a vein, typically in a clinical setting such as an oncology centre. Administration is performed by qualified healthcare professionals following aseptic technique.

The most serious risks include severe neutropenia that can lead to infection, pulmonary toxicity such as interstitial pneumonitis, and rare hypersensitivity reactions. Patients should be monitored closely for signs of infection, respiratory difficulty, or allergic responses.

Navelbine is contraindicated in patients with known hypersensitivity to vinorelbine or other Vinca alkaloids, in pregnant women, and in individuals with severe hepatic impairment. Caution is also advised for patients with pre‑existing bone‑marrow suppression or uncontrolled infections.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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