Product image of Lapatinib Teva (Lapatinib) supplied by GNH India

Lapatinib Teva

Active Ingredient:
Lapatinib
Origin:
EU

Lapatinib Teva (Lapatinib)

Lapatinib, the active ingredient in Lapatinib Teva, is a tyrosine kinase inhibitor presented as a tablet for oral use. It treats HER2‑positive metastatic breast cancer and HER2‑positive metastatic gastric cancer in adult patients.

GNH India supplies Lapatinib Teva as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres worldwide.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

Lapatinib is a targeted oral therapy used in HER2‑driven cancers. It is indicated for the following conditions:

  • HER2‑positive metastatic breast cancer: improves progression‑free survival when combined with chemotherapy.
  • HER2‑positive metastatic gastric cancer: used with capecitabine to delay disease progression.
  • HER2‑positive early‑stage breast cancer (adjuvant setting): administered after surgery to reduce recurrence risk.

How It Works

  • Lapatinib binds to the intracellular tyrosine kinase domains of epidermal growth factor receptor (EGFR/ErbB1) and HER2 (ErbB2), preventing autophosphorylation and downstream signaling through the MAPK and PI3K/AKT pathways. This inhibition reduces tumor cell proliferation, survival, and angiogenesis, thereby slowing cancer growth.

Side Effects

Lapatinib may cause a range of adverse reactions, from mild to severe.

Common Side Effects

  • Diarrhea: frequent loose stools, may require hydration.
  • Rash: skin redness, often on trunk or extremities.
  • Nausea: upset stomach, sometimes with vomiting.
  • Fatigue: persistent tiredness affecting daily activities.
  • Hand‑foot syndrome: redness or swelling of palms and soles.
  • Headache: mild to moderate intensity.

Serious or Rare Side Effects

  • Liver toxicity: elevated transaminases, jaundice.
  • Cardiac dysfunction: decreased left‑ventricular ejection fraction.
  • Interstitial lung disease: breathing difficulty, cough.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • QT interval prolongation: risk of arrhythmia.
  • Severe diarrhea leading to dehydration.

Precautions & Warnings

Before initiating Lapatinib, clinicians should consider several safety measures.

  • Liver monitoring: check hepatic enzymes regularly.
  • Cardiac assessment: evaluate baseline ejection fraction and repeat as needed.
  • Skin surveillance: watch for severe rash or mucosal lesions.
  • Diarrhea management: treat early to prevent dehydration.
  • Drug interactions: avoid strong CYP3A4 inhibitors or inducers without dose adjustment.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Lapatinib interacts with several medicines that affect its metabolism or safety profile.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may increase Lapatinib exposure.
  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce efficacy.
  • Antacids containing aluminum or magnesium: can lower absorption if taken simultaneously.

Moderate Interactions (Monitor Closely)

  • Warfarin: may enhance anticoagulant effect, monitor INR.
  • Digoxin: possible increase in serum levels, check cardiac function.
  • Statins metabolized by CYP3A4 (e.g., simvastatin): monitor for muscle toxicity.
  • Proton pump inhibitors: may modestly affect drug levels, observe clinical response.

Frequently Asked Questions

Lapatinib Teva is indicated for HER2‑positive metastatic breast cancer and HER2‑positive metastatic gastric cancer. In both settings it is used in combination with other chemotherapy agents to improve disease control and delay progression.

Lapatinib blocks the intracellular tyrosine kinase activity of EGFR (ErbB1) and HER2 (ErbB2). By preventing receptor autophosphorylation, it disrupts downstream signaling pathways such as MAPK and PI3K/AKT, which are essential for tumor cell growth and survival.

The specific dose of Lapatinib Teva is determined by the prescribing physician based on the patient’s clinical condition, treatment regimen, and tolerance. Dosage adjustments may be required for drug interactions or organ function changes.

The safety of Lapatinib in pregnancy and lactation has not been established. It is generally advised to avoid use in pregnant or nursing women unless the potential benefit justifies the potential risk to the fetus or infant.

To place an order, 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, and any required import documentation.

Lapatinib is a small‑molecule oral tyrosine kinase inhibitor, whereas agents like trastuzumab and pertuzumab are monoclonal antibodies administered intravenously. Lapatinib offers the convenience of oral dosing and can be combined with different chemotherapy backbones, but its safety profile includes distinct skin and gastrointestinal effects.

Lapatinib Teva tablets should be stored at room temperature, below 25 °C, in the original packaging. Keep the product away from moisture, heat, and direct sunlight to maintain stability.

Lapatinib Teva is taken orally, usually with a low‑fat meal to improve absorption. The tablet should be swallowed whole with water and not crushed or chewed. Dosing schedules are set by the treating oncologist.

Serious risks include liver toxicity, cardiac dysfunction (reduced ejection fraction), severe skin reactions such as Stevens‑Johnson syndrome, interstitial lung disease, and QT interval prolongation. Patients should be monitored regularly for these events, and therapy should be discontinued if they occur.

Lapatinib is contraindicated in patients with known hypersensitivity to the drug or any of its components. It should also be avoided in individuals with severe hepatic impairment, uncontrolled cardiac disease, or those taking strong CYP3A4 inducers without appropriate dose adjustments.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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