GNH USA

Europe — EMA

Navirel (Vinorelbine)

GNH USA supplies Navirel (Vinorelbine), a Vinca alkaloid for non‑small cell lung cancer and breast cancer. Request a quote for global supply to hospitals.

Request sourcing

1
Pack/s

What is Vinorelbine?

Vinorelbine, the active ingredient in Navirel, is a Vinca alkaloid presented as a solution for injection for intravenous use. It treats certain adult cancers, notably non‑small cell lung cancer and breast cancer, by interfering with cell division.

GNH USA supplies Navirel as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres worldwide.

What is Vinorelbine used for?

Navirel (vinorelbine) is employed in oncology for malignancies that rely on rapid cell division. - Non‑small cell lung cancer: improves disease control and overall survival in advanced stages. - Breast cancer (adjuvant setting): used as part of combination regimens to reduce recurrence risk. - Metastatic breast cancer: provides palliation and tumor burden reduction when combined with other agents.

What are the side effects of Vinorelbine?

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

Common Side Effects: - Nausea: mild to moderate gastrointestinal upset. - Vomiting: occasional, may require anti‑emetic support. - Neutropenia: reduced white blood cell count, increasing infection risk. - Alopecia: hair loss that is usually reversible. - Fatigue: generalized tiredness during treatment cycles. - Constipation: bowel motility changes requiring dietary management.

Serious or Rare Side Effects: - Severe neutropenia with febrile infection: requires immediate medical attention. - Pulmonary toxicity: dyspnoea or interstitial pneumonitis. - Peripheral neuropathy: tingling or numbness of extremities. - Anaphylactic reaction: rare but potentially life‑threatening hypersensitivity. - Cardiac arrhythmia: irregular heart rhythms observed in susceptible patients.

What precautions apply to Vinorelbine?

Before initiating Navirel, clinicians should assess patient suitability and monitor for potential complications. - Blood count monitoring: perform complete blood counts before each cycle to detect neutropenia. - Liver function assessment: evaluate hepatic enzymes as vinorelbine is metabolised hepatically. - Neuropathy evaluation: avoid in patients with pre‑existing peripheral neuropathy. - Cardiac risk review: use cautiously in patients with known cardiac disease or arrhythmias. - Concomitant myelosuppressants: avoid or adjust doses when combined with other bone‑marrow suppressing agents. - Store at 2‑8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Vinorelbine interact with?

Vinorelbine can interact with several drug classes, influencing efficacy or toxicity.

Major Interactions (Avoid): - Concurrent vinca alkaloids: additive myelosuppression. - Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): increase vinorelbine exposure. - Live vaccines: risk of infection due to immunosuppression.

Moderate Interactions (Monitor Closely): - CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce therapeutic levels. - Anticoagulants (warfarin, DOACs): enhanced bleeding risk. - Diuretics: potential for electrolyte disturbances when combined with vinorelbine‑induced nausea.

Frequently asked questions

What is Navirel used for?+
Navirel contains vinorelbine, an antineoplastic agent indicated for the treatment of adult patients with non‑small cell lung cancer and breast cancer, typically in advanced or metastatic settings where chemotherapy is required.
How does vinorelbine work?+
Vinorelbine interferes with microtubule assembly by binding to tubulin, preventing the formation of the mitotic spindle. This halts cell division in the M phase, leading to apoptosis of rapidly proliferating cancer cells.
What is the usual dose of Navirel?+
The specific dose and schedule of Navirel are determined by the prescribing oncologist based on the patient’s condition, body surface area, and treatment protocol. Dosing is individualized and not standardized in public information.
Is Navirel safe during pregnancy or breastfeeding?+
Vinorelbine is classified as contraindicated in pregnancy because it may cause fetal harm. Breastfeeding is not recommended while receiving vinorelbine, as the drug can be excreted in milk and affect the infant.
How do I order Navirel from GNH USA?+
To place an order, submit an enquiry on the Navirel product page at gnh-usa.com, specifying the required quantity. GNH USA 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.
How does Navirel compare with other chemotherapy options?+
Compared with other vinca alkaloids such as vincristine, vinorelbine has a distinct toxicity profile, showing lower neurotoxicity but higher myelosuppression. It is often chosen for lung and breast cancer regimens where its efficacy and side‑effect balance align with treatment goals.
What are the storage and handling requirements for Navirel?+
Navirel should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen or shaken. Prior to administration, the solution should be inspected for particulate matter and used within the time frame recommended by the manufacturer.
How is Navirel administered?+
Navirel is supplied as a sterile solution for injection and is administered intravenously by a qualified healthcare professional, typically as an infusion over a prescribed period, following aseptic technique and appropriate dilution guidelines.
What are the most serious risks associated with Navirel?+
The most serious risks include severe neutropenia leading to infection, pulmonary toxicity such as interstitial pneumonitis, and rare anaphylactic reactions. Patients should be monitored closely for signs of infection, respiratory distress, or allergic response during therapy.
Who should not receive Navirel?+
Navirel is contraindicated in patients with known hypersensitivity to vinorelbine or other vinca alkaloids, in pregnant women, and in individuals with severe bone‑marrow suppression or uncontrolled cardiac disease. Clinicians must evaluate each patient’s medical history before initiating therapy.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Vinorelbine
Route
Intravenous Use
Manufacturer
Medac Gesellschaft Für Klinische Spezialpräparate Mbh (Wedel)
Origin
EU

Related products