Product image of Navirel (Vinorelbine) supplied by GNH India

Navirel

Active Ingredient:
Vinorelbine
Origin:
EU

Navirel (Vinorelbine)

Vinorelbine, the active ingredient in Navirel, is a Vinca alkaloid presented as an intravenous solution for intravenous use. It is indicated for the treatment of certain adult solid tumours, most notably non‑small cell lung cancer and breast cancer, where it acts to inhibit cell division.

GNH India supplies Navirel as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres worldwide. The company provides regulatory‑approved product batches to hospitals, pharmacies and procurement teams across the European Union and other global markets.

Manufacturer / TM Owner

Medac Gesellschaft Für Klinische Spezialpräparate Mbh (Wedel)

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Indications & Clinical Uses

Vinorelbine is used in oncology for the management of solid tumours that respond to microtubule inhibition.

  • Non‑small cell lung cancer: improves disease control and overall survival as part of first‑line or second‑line chemotherapy regimens.
  • Breast cancer: used in combination protocols to reduce tumour burden and delay progression in metastatic or adjuvant settings.
  • Combination therapy for solid tumours: incorporated with other chemotherapeutic agents to enhance antitumour activity in approved regimens.

How It Works

  • Vinorelbine binds to the tubulin protein, preventing microtubule polymerisation and thereby disrupting mitotic spindle formation. This blockade arrests dividing cells in the M‑phase of the cell cycle, leading to apoptosis of rapidly proliferating cancer cells while sparing most non‑dividing normal tissues.

Side Effects

Vinorelbine may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Neutropenia: reduced white blood cell count increasing infection risk.
  • Nausea: feeling of sickness often accompanied by vomiting.
  • Fatigue: persistent tiredness affecting daily activities.
  • Alopecia: hair loss that may be temporary.

Serious or Rare Side Effects

  • Severe neutropenia with fever: can lead to life‑threatening infections.
  • Peripheral neuropathy: nerve damage causing numbness or tingling.
  • Pulmonary toxicity: inflammation or fibrosis of lung tissue.

Precautions & Warnings

When using Navirel, clinicians should observe several safety measures to minimise risks.

  • Monitor blood counts: perform regular complete blood count tests to detect neutropenia or anemia.
  • Assess liver function: evaluate hepatic enzymes before and during therapy as vinorelbine is metabolised hepatically.
  • Evaluate cardiac status: consider baseline ECG in patients with cardiac disease.
  • Avoid in active severe infection: postpone treatment if uncontrolled infection is present.
  • Use with caution in renal impairment: adjust dosing if renal function is compromised.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Vinorelbine can interact with other medicines, affecting its efficacy or safety.

Major Interactions (Avoid)

  • Concurrent myelosuppressive agents: combined use markedly increases risk of severe bone‑marrow suppression.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): can raise vinorelbine plasma levels and toxicity.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce drug exposure and effectiveness.
  • Antiemetics containing serotonin antagonists: may alter nausea control and require dose adjustment.
  • Warfarin: vinorelbine may enhance anticoagulant effect, necessitating INR monitoring.

Frequently Asked Questions

Navirel contains vinorelbine, an antineoplastic agent indicated for treatment of adult patients with non‑small cell lung cancer and breast cancer, typically as part of combination chemotherapy regimens.

Vinorelbine binds to tubulin, inhibiting microtubule polymerisation, which prevents formation of the mitotic spindle, arrests cells in M‑phase and leads to apoptosis of rapidly dividing cancer cells.

The dosage of Navirel is determined individually by the prescribing oncologist based on factors such as cancer type, treatment protocol, patient weight, organ function and prior therapy; no standard dose is provided here.

Safety of vinorelbine in pregnancy or lactation has not been established; it is generally contraindicated in pregnant women and should be avoided during breastfeeding unless the benefits outweigh potential risks as assessed by the treating physician.

To place an order, submit an enquiry on the Navirel 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.

Navirel is a vinorelbine‑based intravenous formulation comparable in efficacy to other vinorelbine brands, but differences may exist in excipients, packaging, and supply chain logistics; clinicians may choose based on availability, cost and regulatory status.

Navirel must be stored at 2–8 °C, protected from light, and kept in its original container; it should not be frozen or shaken, and any unused portion should be discarded according to local pharmacy guidelines.

Navirel is given as an intravenous infusion by a qualified healthcare professional, typically diluted in a compatible solution and infused over a prescribed period, following aseptic technique and monitoring for infusion‑related reactions.

The most serious risks include severe neutropenia with febrile infection, pulmonary toxicity, and peripheral neuropathy; patients should be monitored closely for signs of infection, respiratory symptoms and neurological changes throughout therapy.

Navirel is contraindicated in patients with known hypersensitivity to vinorelbine or any formulation components, those with uncontrolled severe infections, and individuals with significant bone‑marrow suppression or organ dysfunction where the risk outweighs benefit.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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