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 targets HER2-positive metastatic breast cancer and HER2-positive 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 Pharmaceuticals Slovakia S.R.O

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Indications & Clinical Uses

Lapatinib is indicated for cancers driven by HER2 signaling and is used as part of combination regimens.

  • HER2‑positive metastatic breast cancer: used with chemotherapy to delay disease progression.
  • HER2‑positive gastric cancer: combined with chemotherapy to improve response rates.

How It Works

  • Lapatinib reversibly inhibits the intracellular tyrosine kinase domains of epidermal growth factor receptor (EGFR/ErbB1) and HER2/neu (ErbB2). By blocking these receptors, it suppresses downstream signaling pathways such as MAPK and PI3K/AKT, reducing tumor cell proliferation and survival.

Side Effects

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

Common Side Effects

  • Diarrhea
  • Rash or acne‑like skin eruption
  • Nausea and vomiting
  • Fatigue
  • Hand‑foot syndrome
  • Headache

Serious or Rare Side Effects

  • Hepatotoxicity (elevated liver enzymes, hepatitis)
  • QT interval prolongation leading to cardiac arrhythmia
  • Severe skin reactions such as Stevens‑Johnson syndrome
  • Interstitial lung disease or pneumonitis
  • Severe diarrhea leading to dehydration
  • Cardiac dysfunction or heart failure

Precautions & Warnings

Before initiating therapy, clinicians should assess baseline health status and monitor patients regularly.

  • Cardiac monitoring: evaluate baseline ejection fraction and repeat as clinically indicated.
  • Liver function: obtain baseline hepatic enzymes and monitor periodically.
  • Electrolyte balance: check potassium and magnesium levels, especially if diarrhea occurs.
  • Drug interactions: avoid concomitant use of strong CYP3A4 inhibitors.
  • Pregnancy and lactation: use only if potential benefit justifies potential risk; discuss with patient.
  • Store at ambient temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Lapatinib interacts with several drug classes that may alter its exposure or increase toxicity.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole) – may raise plasma levels.
  • Concurrent QT‑prolonging agents – increase risk of cardiac arrhythmia.
  • Paclitaxel or other taxanes – may amplify hematologic toxicity.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin, carbamazepine) – may reduce efficacy.
  • Antacids containing aluminum or magnesium – may affect absorption; separate dosing by at least 2 hours.
  • Warfarin – monitor INR for potential changes.
  • Digoxin – observe serum levels for possible alteration.

Frequently Asked Questions

Lapatinib Teva is prescribed for adult patients with HER2‑positive metastatic breast cancer and HER2‑positive gastric cancer. In both indications it is used as part of a combination regimen with chemotherapy to inhibit tumor growth driven by HER2 signaling.

Lapatinib blocks the intracellular tyrosine kinase activity of EGFR (ErbB1) and HER2 (ErbB2). This inhibition prevents activation of downstream pathways such as MAPK and PI3K/AKT, which are essential for cancer cell proliferation and survival, thereby slowing disease progression.

The specific dose and schedule of Lapatinib Teva are determined by the treating physician based on the patient’s clinical condition, concomitant therapies, and tolerability. Prescribers follow approved labeling and clinical guidelines to individualise therapy.

Safety data for Lapatinib in pregnancy and lactation are limited. It should only be used if the potential benefit outweighs the potential risk to the fetus or infant, and the decision must be made by a qualified healthcare professional after thorough counseling.

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 necessary import documentation.

Lapatinib is a small‑molecule tyrosine kinase inhibitor that can be taken orally, whereas agents like trastuzumab and pertuzumab are monoclonal antibodies administered intravenously. Lapatinib offers the advantage of oral dosing and can be combined with certain chemotherapies, but its safety profile and efficacy differ, requiring individualized treatment decisions.

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

Lapatinib Teva is taken orally, usually once daily, with or without food as directed by the prescribing clinician. The tablet should be swallowed whole with a glass of water and not chewed or crushed.

Serious risks include hepatotoxicity, severe skin reactions such as Stevens‑Johnson syndrome, QT interval prolongation leading to cardiac arrhythmias, interstitial lung disease, and significant diarrhea that can cause dehydration. Patients should be monitored closely for these events.

Lapatinib is contraindicated in patients with known hypersensitivity to the drug or any of its excipients. Caution is advised for individuals with pre‑existing severe cardiac disease, uncontrolled liver dysfunction, or those taking strong CYP3A4 inhibitors without appropriate dose adjustments.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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