GNH USA

Europe — EMA

Lenvima

GNH USA supplies Lenvima (lenvatinib), a tyrosine kinase inhibitor for differentiated thyroid carcinoma, renal cell carcinoma, hepatocellular carcinoma

Lenvatinib

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What is Lenvatinib?

lenvatinib, the active ingredient in Lenvima, is a tyrosine kinase inhibitor presented as an oral tablet for oral use. It is indicated for several advanced solid tumours and is prescribed by oncologists for adult patients with specific cancer types. GNH USA supplies Lenvima as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

What is Lenvatinib used for?

Lenvima targets multiple signalling pathways that drive tumour growth and angiogenesis, making it useful in several solid‑tumour indications. - Differentiated thyroid carcinoma: helps control disease progression in patients with radioactive iodine‑refractory disease. - Renal cell carcinoma: used in combination with everolimus to improve progression‑free survival. - Hepatocellular carcinoma: administered as first‑line therapy for unresectable disease. - Endometrial carcinoma: combined with pembrolizumab for advanced or recurrent cases.

What are the side effects of Lenvatinib?

Lenvima may cause a range of adverse reactions, which vary in frequency and severity.

Common Side Effects: - Hypertension: elevated blood pressure requiring monitoring. - Diarrhoea: may be mild to moderate. - Fatigue: persistent tiredness. - Nausea: occasional upset stomach. - Decreased appetite: reduced food intake. - Proteinuria: presence of protein in urine.

Serious or Rare Side Effects: - Hepatotoxicity: liver enzyme elevations or failure. - Cardiac dysfunction: reduced left‑ventricular ejection fraction. - Thromboembolic events: blood clots in veins or arteries. - Gastrointestinal perforation: rare but severe bowel injury. - Severe haemorrhage: uncontrolled bleeding. - Renal failure: impaired kidney function.

What precautions apply to Lenvatinib?

Before initiating Lenvima, clinicians should assess patient risk factors and monitor relevant parameters. - Blood pressure monitoring: check regularly and treat hypertension promptly. - Liver function tests: evaluate baseline and periodic hepatic enzymes. - Cardiac assessment: perform echocardiogram if history of heart disease. - Pregnancy risk: avoid use in pregnancy; discuss contraception. - Store at ambient temperature: keep below 25 °C, in original packaging, protected from moisture and light.

What does Lenvatinib interact with?

Lenvima can interact with several drug classes, influencing efficacy or safety.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole): may increase lenvatinib exposure. - Anticoagulants (e.g., warfarin): heightened risk of bleeding. - High‑dose aspirin or NSAIDs: increased gastrointestinal bleeding risk.

Moderate Interactions (Monitor Closely): - CYP3A4 inducers (e.g., rifampin): may reduce drug levels. - Diuretics: may exacerbate hypertension. - Hormonal contraceptives: potential reduced effectiveness.

Frequently asked questions

What conditions is Lenvima used to treat?+
Lenvima (lenvatinib) is prescribed for adult patients with differentiated thyroid carcinoma that is refractory to radioactive iodine, advanced renal cell carcinoma, unresectable hepatocellular carcinoma, and advanced or recurrent endometrial carcinoma, often in combination with other targeted agents.
How does lenvatinib work in the body?+
Lenvatinib blocks multiple receptor tyrosine kinases such as VEGFR, FGFR, PDGFRα, RET and KIT. Inhibiting these pathways reduces tumour blood‑vessel formation, slows cell proliferation, and promotes cancer cell death, thereby limiting tumour growth.
What is the usual dose of Lenvima?+
The specific dose of Lenvima is determined by the treating physician based on the patient’s cancer type, disease stage, renal and hepatic function, and other clinical factors. Patients should follow the prescribing information provided by their healthcare professional.
Is Lenvima safe to use during pregnancy or breastfeeding?+
Lenvima is classified as Pregnancy Category D, indicating evidence of risk to the fetus. It should not be used during pregnancy, and effective contraception is required. Safety during breastfeeding has not been established, so breastfeeding is generally discouraged while on therapy.
How do I order Lenvima from GNH USA?+
To request Lenvima, submit an enquiry on the 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 and any necessary import documentation.
How does Lenvima compare with other tyrosine kinase inhibitors?+
Lenvima uniquely targets both VEGFR and FGFR families, offering broader inhibition of angiogenic pathways compared with some TKIs that focus mainly on VEGFR. This broader spectrum can be advantageous in tumours driven by multiple growth factors, though safety profiles differ and should be evaluated individually.
What are the recommended storage conditions for Lenvima?+
Lenvima tablets should be stored at ambient temperature, below 25 °C, in the original container to protect from moisture and light. Keep the medication out of reach of children and do not use if the packaging is damaged.
How is Lenvima administered to patients?+
Lenvima is taken orally as a tablet, usually once daily on an empty stomach (at least one hour before or two hours after a meal). Patients should swallow the tablet whole with water and follow any specific instructions from their prescriber.
What are the most serious risks associated with Lenvima therapy?+
Serious risks include severe hypertension, liver toxicity, cardiac dysfunction, thromboembolic events, gastrointestinal perforation, and severe bleeding. Patients should be monitored regularly for these events, and therapy should be adjusted or discontinued if serious adverse reactions occur.
Who should not use Lenvima?+
Lenvima is contraindicated in patients with known hypersensitivity to lenvatinib or any of its excipients. It should also be avoided in pregnant women and used with caution in patients with uncontrolled hypertension, significant liver impairment, or severe cardiac disease.
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
Lenvatinib
Route
Oral Use
Manufacturer
Eisai Gmbh
Origin
EU

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