Product image of Lenvima (Lenvatinib) supplied by GNH India

Lenvima

Active Ingredient:
Lenvatinib
Origin:
EU

Lenvima (Lenvatinib)

Lenvatinib, the active ingredient in Lenvima, is a tyrosine kinase inhibitor presented as a tablet for oral use. It treats certain advanced cancers such as differentiated thyroid cancer, renal cell carcinoma, hepatocellular carcinoma, and endometrial carcinoma in adult patients.

GNH India supplies Lenvima as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Eisai Gmbh

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Indications & Clinical Uses

  • Lenvima (lenvatinib) is used in oncology to target tumors that rely on multiple growth‑factor pathways.
  • Radioiodine‑refractory differentiated thyroid cancer: prolongs progression‑free survival in adult patients.
  • Advanced renal cell carcinoma: improves overall survival when used alone or with pembrolizumab.
  • Unresectable hepatocellular carcinoma: delays tumor growth in patients not eligible for surgery.
  • Advanced endometrial carcinoma: provides disease control after prior systemic therapy.

How It Works

  • Lenvatinib inhibits multiple receptor tyrosine kinases—including VEGFR1‑3, FGFR1‑4, PDGFRα, RET and KIT—thereby blocking angiogenesis, tumor cell proliferation, and survival signaling pathways that drive cancer growth.

Side Effects

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

Common Side Effects

  • Hypertension: elevated blood pressure often requiring monitoring or medication.
  • Diarrhea: watery stools that may lead to dehydration.
  • Fatigue: persistent tiredness affecting daily activities.
  • Decreased appetite: reduced desire to eat, potentially causing weight loss.

Serious or Rare Side Effects

  • Hepatic failure: signs of liver dysfunction such as jaundice or elevated enzymes.
  • Cardiac ischemia: chest pain or heart‑attack symptoms.
  • Gastrointestinal perforation: severe abdominal pain and infection risk.
  • Severe hemorrhage: uncontrolled bleeding, including nosebleeds or gastrointestinal bleeding.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate several safety parameters.

  • Blood pressure monitoring: check regularly and manage hypertension promptly.
  • Liver function tests: assess baseline and periodic hepatic enzymes.
  • Cardiac evaluation: perform ECG and assess for ischemic disease before starting.
  • Pregnancy risk: avoid use in pregnancy; drug is Category D.
  • Drug interactions: review concomitant medications for CYP3A4 substrates.
  • Store at ambient temperature: keep below 25°C in original packaging, protect from moisture.

Avoid Interactions

Lenvima interacts with several medicines; some combinations should be avoided while others require close observation.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce lenvatinib exposure.
  • Anticoagulants (e.g., warfarin, direct oral anticoagulants): increased risk of bleeding.
  • High‑dose aspirin or NSAIDs: may exacerbate bleeding risk.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., fluconazole, erythromycin): may increase plasma levels.
  • Diuretics: may potentiate hypertension.
  • Levothyroxine: may require dose adjustment due to altered thyroid hormone metabolism.

Frequently Asked Questions

Lenvima (lenvatinib) is approved for several advanced solid tumours, including radioiodine‑refractory differentiated thyroid cancer, advanced renal cell carcinoma, unresectable hepatocellular carcinoma, and advanced endometrial carcinoma that have progressed after prior therapy.

Lenvatinib blocks multiple receptor tyrosine kinases such as VEGFR1‑3, FGFR1‑4, PDGFRα, RET and KIT. By inhibiting these pathways it reduces tumour blood‑vessel formation, cell proliferation and survival signals, thereby slowing or halting cancer growth.

The prescribed dose of Lenvima is individualized by the treating physician based on the specific indication, patient weight, renal and hepatic function, and any concomitant medications. No fixed regimen is provided here; dosing decisions are made by qualified healthcare professionals.

Lenvima is classified as Pregnancy Category D, indicating evidence of risk to the fetus. It should not be used during pregnancy, and women of child‑bearing potential must use effective contraception. Limited data exist for breastfeeding, so use is generally discouraged while nursing.

To request Lenvima, 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 any cold‑chain needs) and required import documentation.

Lenvima uniquely targets a broad spectrum of kinases (VEGFR, FGFR, PDGFRα, RET, KIT), offering activity against tumours that rely on multiple growth‑factor pathways. Compared with more selective TKIs, lenvatinib may provide broader anti‑angiogenic effects but also carries a distinct safety profile that requires careful monitoring.

Lenvima tablets should be stored at ambient temperature, below 25 °C, in the original blister pack or container. Keep the product away from moisture and direct sunlight to maintain stability throughout its shelf life.

Lenvima is taken orally as a whole tablet, with or without food. Patients should swallow the tablet whole with water and follow the prescribing physician’s instructions regarding timing and any necessary dose adjustments.

Serious adverse events include severe hypertension, hepatic failure, cardiac ischemia, gastrointestinal perforation, and major bleeding. Patients should be monitored regularly for blood pressure, liver function, cardiac symptoms and any signs of gastrointestinal complications.

Lenvima is contraindicated in patients with severe hepatic impairment, uncontrolled hypertension, known hypersensitivity to lenvatinib, and in pregnant women. Caution is also advised for individuals with recent major cardiovascular events or active bleeding disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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