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 employed in the treatment of certain solid tumours, notably non‑small cell lung cancer and metastatic breast cancer, in adult patients who require systemic chemotherapy.

GNH India supplies Navirel as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres worldwide. The company adheres to EU quality standards and provides reliable logistics for hospitals, pharmacies and procurement teams across multiple regions, 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 a Vinca alkaloid used in the management of solid tumours by disrupting microtubule formation.
  • Non‑small cell lung cancer: improves disease control and overall survival in eligible adult patients.
  • Metastatic breast cancer: provides tumor response and disease stabilization in advanced disease.
  • Combination therapy for NSCLC: used with cisplatin to enhance cytotoxic efficacy in first‑line regimens.

How It Works

  • Vinorelbine binds to tubulin at the plus end of microtubules, preventing polymerisation and thereby inhibiting the formation of functional mitotic spindles. This blockade arrests cells in the G2/M phase of the cell cycle, leading to apoptosis of rapidly dividing cancer cells. The drug’s activity is independent of p53 status and is enhanced when combined with other antimitotic agents, and contributes to tumor shrinkage.

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 leading to infection risk.
  • Nausea and vomiting: gastrointestinal upset commonly reported during treatment.
  • Fatigue: persistent tiredness affecting daily activities.
  • Alopecia: hair loss that may be temporary or reversible.

Serious or Rare Side Effects

  • Severe neutropenia with febrile infection: life‑threatening immune suppression.
  • Pulmonary toxicity: interstitial pneumonitis or fibrosis requiring medical intervention.
  • Anaphylactic reactions: acute hypersensitivity that may need emergency treatment.

Precautions & Warnings

When using Vinorelbine, clinicians should observe specific precautions to minimise risks and optimise patient safety.

  • Monitor blood counts: perform regular complete blood count tests to detect neutropenia or anemia.
  • Assess hepatic function: evaluate liver enzymes before and during therapy as metabolism is hepatic.
  • Evaluate for hypersensitivity: watch for signs of allergic reaction during infusion.
  • Use caution in neuropathy: patients with pre‑existing peripheral neuropathy may experience worsening symptoms.
  • Avoid concurrent strong CYP3A4 inhibitors: drugs such as ketoconazole can increase vinorelbine exposure.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Vinorelbine interacts with several medicines; understanding the level of interaction guides clinical management.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may raise vinorelbine plasma levels and toxicity.
  • Concurrent myelosuppressive agents (e.g., cyclophosphamide): increase risk of severe bone‑marrow suppression.
  • Live vaccines: immunosuppression can reduce vaccine efficacy and increase infection risk.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin, phenytoin): may lower vinorelbine exposure, reducing efficacy.
  • Anticoagulants (e.g., warfarin): vinorelbine can affect coagulation parameters, requiring INR monitoring.
  • Other vinca alkaloids (e.g., vincristine): additive neurotoxicity risk warrants dose adjustment.

Frequently Asked Questions

Navirel contains vinorelbine, which is indicated for the treatment of adult patients with non‑small cell lung cancer and metastatic breast cancer. It is administered as part of a systemic chemotherapy regimen to control tumor growth and improve survival outcomes.

Vinorelbine interferes with microtubule dynamics by binding to tubulin, preventing polymerisation. This halts mitotic spindle formation, arrests cells in the G2/M phase, and triggers apoptosis of rapidly dividing cancer cells, thereby reducing tumor proliferation.

The dosage of Navirel is individualized. A qualified prescriber determines the appropriate dose, infusion rate, and treatment schedule based on the patient’s condition, body surface area, and clinical response.

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. Consultation with a healthcare professional is essential.

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, vinorelbine offers a distinct toxicity profile, with relatively lower neurotoxicity but higher rates of neutropenia. It is often chosen for patients who may not tolerate agents such as vincristine, and can be combined with platinum‑based drugs for synergistic effect.

Navirel should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. The solution should be kept in its original packaging until use and inspected for particulate matter before administration.

Navirel is supplied as an intravenous solution and is administered by slow infusion into a peripheral or central vein under the supervision of qualified medical personnel. Infusion time and rate are determined by the prescribing physician.

The most serious risks include severe neutropenia with febrile infection, pulmonary toxicity such as interstitial pneumonitis, and anaphylactic reactions. Prompt monitoring and supportive care are essential to manage these potential complications.

Navirel is contraindicated in patients with known hypersensitivity to vinorelbine or other vinca alkaloids, in those with severe bone‑marrow suppression, and in pregnant women. Caution is advised for patients with significant hepatic impairment or pre‑existing neuropathy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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