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 an oral formulation for oral use. It is employed in the treatment of certain advanced solid tumours, notably 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

Navelbine is a chemotherapy agent used in the management of solid tumours that rely on microtubule inhibition.

  • Non‑small cell lung cancer: improves disease control and overall survival when combined with standard regimens.
  • Metastatic breast cancer: provides tumour reduction and symptom relief in patients with prior therapy.
  • Advanced or recurrent solid tumours: may be considered as part of combination protocols when other options are limited.

How It Works

  • Vinorelbine binds to tubulin at the Vinca binding site, preventing microtubule polymerisation. This disrupts the mitotic spindle, causing cell‑cycle arrest in the M phase and ultimately triggering apoptosis of rapidly dividing cancer cells. The drug’s activity is independent of DNA synthesis and is selective for proliferating tumour cells.

Side Effects

Vinorelbine is associated with a range of adverse reactions that vary in frequency and severity.

Common Side Effects

  • Neutropenia: reduced white blood cell count increasing infection risk.
  • Anemia: decreased red blood cells causing fatigue.
  • Nausea and vomiting: gastrointestinal upset common after oral dosing.
  • Constipation: bowel motility reduction.
  • Fatigue: generalised tiredness.
  • Alopecia: hair thinning or loss.

Serious or Rare Side Effects

  • Severe neutropenia with febrile infection.
  • Pulmonary toxicity, including interstitial pneumonitis.
  • Peripheral neuropathy: tingling or numbness in extremities.
  • Allergic reactions: rash, pruritus, or anaphylaxis.
  • Cardiac arrhythmias: irregular heart rhythms.
  • Hepatic dysfunction: elevated liver enzymes or jaundice.

Precautions & Warnings

Before initiating therapy, clinicians should assess baseline organ function and monitor patients closely.

  • Monitor blood counts: perform regular complete blood counts to detect myelosuppression.
  • Assess liver function: check hepatic enzymes and bilirubin prior to each cycle.
  • Evaluate pulmonary status: avoid use in patients with pre‑existing severe lung disease.
  • Use caution in the elderly: dose adjustments may be required due to reduced clearance.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Vinorelbine may interact with several drug classes, requiring careful management.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): increase vinorelbine exposure.
  • Strong CYP3A4 inducers (e.g., rifampicin, carbamazepine): reduce therapeutic levels.
  • Concurrent myelosuppressive chemotherapy: markedly heighten bone‑marrow toxicity.

Moderate Interactions (Monitor Closely)

  • Antiemetics such as ondansetron: may affect QT interval.
  • Anticoagulants (e.g., warfarin): monitor coagulation parameters.
  • Diuretics: watch for electrolyte disturbances.
  • CYP2D6 substrates: potential modest effect on metabolism.

Frequently Asked Questions

Navelbine (vinorelbine tartrate) is indicated for the treatment of adult patients with non‑small cell lung cancer and metastatic breast cancer. It is used as part of combination chemotherapy regimens to control tumour growth, improve response rates, and extend survival in these advanced solid‑tumour settings.

Vinorelbine interferes with microtubule dynamics by binding to tubulin at the Vinca site, preventing polymerisation. This halts mitotic spindle formation, arrests cells in the M phase of the cell cycle, and triggers programmed cell death (apoptosis) in rapidly dividing cancer cells.

The specific dose of Navelbine is determined by the prescribing oncologist based on the patient’s cancer type, prior therapies, organ function, and overall health. Dosing is individualized and may be adjusted during treatment according to response and tolerance.

There is limited clinical data on vinorelbine use in pregnancy, and the drug is generally contraindicated because of potential fetal toxicity. Breastfeeding is not recommended while receiving vinorelbine, as the medication can be excreted in milk and may harm the infant.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity of Navelbine. 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.

Compared with vincristine, vinorelbine has a higher affinity for tubulin and is administered orally, offering greater convenience. Its toxicity profile differs, with vinorelbine causing more neutropenia but less neurotoxicity than vincristine. Choice of agent depends on tumour type, prior treatment history, and individual patient tolerance.

Navelbine tablets should be stored at ambient temperature, below 25 °C, in the original packaging to protect from moisture and light. Keep the product out of reach of children and avoid exposure to excessive heat or humidity.

Navelbine is taken orally with a glass of water, preferably on an empty stomach unless otherwise directed by the prescriber. It may be given with anti‑emetic medication to reduce nausea, and patients should follow the dosing schedule prescribed by their oncologist.

The most critical risks include severe neutropenia leading to infection, pulmonary toxicity such as interstitial pneumonitis, and rare but serious allergic reactions. Patients should report fever, persistent cough, shortness of breath, or any signs of infection promptly to their healthcare provider.

Navelbine is contraindicated in patients with known hypersensitivity to vinorelbine or other Vinca alkaloids, those with severe bone‑marrow suppression, uncontrolled infections, or significant pre‑existing pulmonary disease. Caution is also advised for individuals with impaired hepatic function.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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