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 injectable solution for intravenous use. It is employed in the treatment of certain advanced solid tumours, notably non‑small cell lung cancer and metastatic breast cancer, in adult oncology patients.

GNH India supplies Navirel as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres worldwide. The company adheres to stringent quality standards and provides reliable logistics for hospital pharmacies and cancer treatment facilities across global markets, ensuring timely delivery and regulatory compliance.

Manufacturer / TM Owner

Medac Gesellschaft Für Klinische Spezialpräparate Mbh (Wedel)

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Indications & Clinical Uses

  • Vinorelbine is indicated for specific solid tumour types within the oncology therapeutic pathway.
  • Non‑small cell lung cancer: used to improve progression‑free survival in adult patients with advanced disease.
  • Metastatic breast cancer: employed to control disease progression in patients previously treated with anthracyclines and taxanes.

How It Works

  • Vinorelbine binds to tubulin at the Vinca binding site, inhibiting microtubule polymerisation. This disruption prevents the formation of functional mitotic spindles, leading to cell‑cycle arrest in the M phase and ultimately triggering 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 common after infusion.
  • Fatigue: persistent tiredness affecting daily activities.
  • Alopecia: hair loss that may be temporary.
  • Constipation: decreased bowel movements.
  • Anemia: lowered red blood cell levels causing weakness.

Serious or Rare Side Effects

  • Febrile neutropenia: fever with low neutrophils requiring urgent care.
  • Severe pulmonary toxicity: breathlessness or interstitial pneumonitis.
  • Peripheral neuropathy: tingling or numbness in extremities.
  • Cardiac toxicity: arrhythmias or reduced cardiac function.
  • Anaphylactic reactions: severe allergic response needing immediate treatment.
  • Thrombocytopenia: low platelet count leading to bleeding risk.

Precautions & Warnings

  • Vinorelbine requires careful monitoring and specific safety measures before and during therapy.
  • Monitor blood counts: perform regular CBCs to detect neutropenia and anemia.
  • Assess liver function: adjust dosing in patients with hepatic impairment.
  • Avoid concurrent myelosuppressive agents: reduce risk of severe bone‑marrow suppression.
  • Use anti‑emetics prophylactically: mitigate nausea and vomiting associated with infusion.
  • Pregnancy and lactation: contraindicated unless benefits outweigh potential risks.
  • 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 safety and efficacy.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): increase vinorelbine exposure.
  • Potent CYP3A4 inducers (e.g., rifampin, carbamazepine): reduce therapeutic levels.
  • Concurrent myelosuppressive chemotherapy: heighten risk of severe neutropenia.
  • Live vaccines: risk of infection due to immunosuppression.
  • Other Vinca alkaloids: additive neurotoxicity.

Moderate Interactions (Monitor Closely)

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

Frequently Asked Questions

Navirel contains vinorelbine, an antineoplastic agent used primarily to treat advanced non‑small cell lung cancer and metastatic breast cancer in adult patients, often after prior chemotherapy regimens.

Vinorelbine binds to tubulin, preventing microtubule assembly during mitosis. This blocks cell‑division in the M phase, leading to apoptosis of rapidly proliferating cancer cells.

The dosing regimen for Navirel is individualized by the prescribing oncologist based on factors such as cancer type, patient weight, renal and hepatic function, and prior treatments.

Vinorelbine is classified as contraindicated in pregnancy and breastfeeding because of potential fetal toxicity and excretion in milk. It should only be used if the potential benefit justifies the risk.

To request Navirel, 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, with more pronounced myelosuppression but less neurotoxicity. It is often chosen when patients have progressed after anthracycline or taxane therapy.

Navirel should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. Use aseptic technique when preparing the intravenous solution and discard any unused portion after the recommended time.

Navirel is given as an intravenous infusion, typically over 6–10 minutes. The infusion is performed by qualified healthcare professionals in a clinical setting, with monitoring for infusion‑related reactions.

The most serious risks include severe neutropenia with fever (febrile neutropenia), pulmonary toxicity, and rare but life‑threatening allergic reactions. Prompt medical attention is required if these symptoms occur.

Navirel is contraindicated in patients with known hypersensitivity to vinorelbine or other Vinca alkaloids, in those with severe bone‑marrow suppression, and in pregnant or breastfeeding women unless the benefits outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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