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

Lapatinib Stada

Active Ingredient:
Lapatinib
Origin:
EU

Lapatinib Stada (Lapatinib)

Lapatinib, the active ingredient in Lapatinib Stada, is a Tyrosine kinase inhibitor presented as a tablet for Oral use. It treats HER2‑positive metastatic breast cancer and HER2‑positive advanced gastric or gastro‑oesophageal junction adenocarcinoma in adult patients.

GNH India supplies Lapatinib Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres, hospitals and pharmacies worldwide.

Manufacturer / TM Owner

Stadapharm Gmbh

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Indications & Clinical Uses

Lapatinib acts on the HER2 signaling pathway, providing targeted therapy for specific cancers.

  • HER2‑positive metastatic breast cancer: improves progression‑free and overall survival.
  • HER2‑positive advanced gastric cancer: delays disease progression and extends survival.
  • HER2‑positive gastro‑oesophageal junction adenocarcinoma: contributes to tumor control in combination regimens.

How It Works

  • Lapatinib reversibly inhibits the intracellular tyrosine kinase activity of both epidermal growth factor receptor (EGFR/ErbB1) and HER2/neu (ErbB2). By blocking these receptors, it prevents downstream signaling through the MAPK and PI3K/AKT pathways, thereby reducing cellular proliferation, survival, and angiogenesis in tumor cells that overexpress HER2.

Side Effects

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

Common Side Effects

  • Diarrhea: frequent loose stools.
  • Rash: skin redness or acne‑like eruptions.
  • Nausea: feeling of sickness, sometimes with vomiting.
  • Fatigue: persistent tiredness.
  • Stomatitis: inflammation of the mouth lining.
  • Elevated liver enzymes: mild transaminase increase.

Serious or Rare Side Effects

  • Interstitial lung disease: breathing difficulties and cough.
  • Severe hepatic failure: jaundice, abdominal pain, elevated bilirubin.
  • Cardiac dysfunction: reduced left‑ventricular ejection fraction.
  • Stevens‑Johnson syndrome: severe skin blistering.
  • Severe skin reactions: toxic epidermal necrolysis.
  • Hemorrhagic events: unusual bleeding or bruising.

Precautions & Warnings

When using Lapatinib, clinicians should observe several safety measures.

  • Cardiac monitoring: assess left‑ventricular function before and during therapy.
  • Liver function tests: check transaminases and bilirubin regularly.
  • Dermatologic assessment: watch for severe rash or skin reactions.
  • Pregnancy avoidance: drug is contraindicated; ensure effective contraception.
  • Dose adjustment: consider hepatic impairment when determining dose.
  • Store below 25°C: keep in the original packaging, protect from moisture and direct light.

Avoid Interactions

Lapatinib can interact with other medicines, altering its effectiveness or safety.

Major Interactions (Avoid)

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

Moderate Interactions (Monitor Closely)

  • Warfarin: may enhance anticoagulant effect, requiring INR monitoring.
  • Digoxin: potential increase in serum concentration.
  • Other HER2‑targeted agents (e.g., trastuzumab): monitor for additive cardiac toxicity.

Frequently Asked Questions

Lapatinib Stada is indicated for HER2‑positive metastatic breast cancer and HER2‑positive advanced gastric or gastro‑oesophageal junction adenocarcinoma in adult patients. It is used as part of a targeted therapy regimen to inhibit tumor growth driven by HER2 signaling.

Lapatinib reversibly blocks the tyrosine kinase activity of both EGFR (ErbB1) and HER2 (ErbB2) receptors. This inhibition stops downstream signaling pathways that promote cancer cell proliferation, survival, and angiogenesis, thereby slowing tumor progression.

The prescribed dose of Lapatinib Stada is determined by the treating physician based on the patient’s clinical condition, concomitant therapies, and individual tolerability. Dosing regimens are individualized and should follow the prescriber’s instructions.

The safety of Lapatinib in pregnancy and lactation has not been established. It is generally contraindicated in pregnant women, and breastfeeding is not recommended while receiving this medication. Effective contraception should be used during treatment.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details, and necessary import documentation.

Lapatinib is a small‑molecule tyrosine kinase inhibitor that targets the intracellular domain of HER2, whereas agents like trastuzumab are monoclonal antibodies that bind the extracellular domain. Lapatinib can be combined with other HER2‑targeted drugs to enhance efficacy, especially in patients with resistance to antibody‑based therapy.

Lapatinib Stada should be stored at temperatures below 25 °C, in its original packaging, protected from moisture and direct sunlight. Maintaining these conditions helps preserve the tablet’s stability and potency.

Lapatinib is taken orally, usually as a tablet swallowed whole with water. It is typically administered once daily, and patients should follow the dosing schedule prescribed by their healthcare provider, including any dietary restrictions.

Serious risks include interstitial lung disease, severe hepatic toxicity, cardiac dysfunction (reduced left‑ventricular ejection fraction), and life‑threatening skin reactions such as Stevens‑Johnson syndrome. Patients should be monitored closely for these events and report any concerning symptoms promptly.

Lapatinib is contraindicated in patients with known hypersensitivity to the drug or its excipients, in pregnant women, and in individuals with severe hepatic impairment without appropriate dose adjustment. Caution is also advised for patients with pre‑existing cardiac disease or significant lung disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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