Product image of Imatinib Eg Labo (Imatinib) supplied by GNH India

Imatinib Eg Labo

Active Ingredient:
Imatinib
Origin:
EU

Imatinib Eg Labo (Imatinib)

Imatinib, the active ingredient in Imatinib Eg Labo, is a tyrosine kinase inhibitor presented as an oral tablet for oral use. It treats chronic myeloid leukemia and gastrointestinal stromal tumor in adult patients by targeting BCR‑ABL driven cell proliferation and related malignant pathways.

GNH India supplies Imatinib Eg Labo as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Eg Labo Laboratoires Eurogenerics

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Indications & Clinical Uses

Imatinib is a tyrosine kinase inhibitor used in hematologic and solid‑tumor indications.

  • Chronic myeloid leukemia: provides disease control by inhibiting BCR‑ABL driven proliferation.
  • Gastrointestinal stromal tumor: induces tumor shrinkage and prolongs progression‑free survival.
  • Philadelphia chromosome‑positive acute lymphoblastic leukemia: offers targeted therapy to improve remission rates.

How It Works

  • Imatinib selectively binds to the ATP‑binding site of the BCR‑ABL fusion protein and other related tyrosine kinases such as c‑KIT and PDGFR. This inhibition blocks downstream signaling pathways that drive malignant cell growth, leading to reduced proliferation and increased apoptosis of cancerous cells.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Edema: peripheral swelling, often in the ankles.
  • Muscle cramps: intermittent skeletal muscle discomfort.
  • Fatigue: generalized tiredness.
  • Diarrhea: loose stools, usually self‑limiting.
  • Rash: mild skin eruption.

Serious or Rare Side Effects

  • Neutropenia: significant reduction in white blood cells.
  • Hepatotoxicity: elevated liver enzymes or liver injury.
  • Cardiac failure: signs of reduced cardiac output.
  • Severe bleeding: gastrointestinal or intracranial hemorrhage.
  • Pulmonary hypertension: elevated pressure in lung arteries.
  • Anaphylaxis: acute allergic reaction requiring emergency care.

Precautions & Warnings

Patients should be monitored for safety and efficacy throughout therapy.

  • Monitor blood counts: perform regular complete blood count assessments.
  • Assess liver function: check hepatic enzymes before and during treatment.
  • Evaluate cardiac status: baseline and periodic echocardiograms for at‑risk patients.
  • Avoid use in known hypersensitivity: discontinue if severe allergic reaction occurs.
  • Counsel on pregnancy risks: discuss potential fetal effects with women of childbearing potential.
  • Store at below 25°C: keep in the original packaging, protect from moisture and light.

Avoid Interactions

Imatinib may interact with several concomitant medicines, requiring clinical attention.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may increase imatinib plasma levels.
  • Potent CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce therapeutic exposure.
  • Antacids containing aluminum or magnesium: can impair absorption if taken simultaneously.

Moderate Interactions (Monitor Closely)

  • CYP3A4 substrates (e.g., warfarin, midazolam): may require dose adjustments.
  • QT‑prolonging agents (e.g., sotalol, quinidine): monitor cardiac rhythm.
  • Vaccines (live attenuated): assess timing relative to therapy.

Frequently Asked Questions

Imatinib Eg Labo is indicated for the treatment of chronic myeloid leukemia, gastrointestinal stromal tumor, and Philadelphia chromosome‑positive acute lymphoblastic leukemia. In each case the drug targets the BCR‑ABL tyrosine kinase that drives malignant cell growth.

Imatinib binds to the ATP‑binding pocket of BCR‑ABL and related kinases such as c‑KIT and PDGFR. This blocks phosphorylation events required for downstream signaling, thereby halting uncontrolled proliferation and promoting apoptosis of cancer cells.

The specific dose and dosing schedule are determined by the prescribing clinician based on the patient’s diagnosis, disease stage, and individual tolerance. Healthcare professionals should follow the latest clinical guidelines and product labeling when prescribing.

Safety data in pregnancy and lactation are limited. Imatinib may pose risks to the fetus and is generally avoided unless the potential benefit outweighs the risk. Breastfeeding is not recommended while receiving the medication. Consultation with a specialist is essential.

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.

Imatinib is a first‑generation BCR‑ABL inhibitor and remains a standard of care for many patients. Newer agents such as dasatinib or nilotinib may offer activity against certain resistant mutations, but Imatinib’s long‑term safety profile and extensive clinical experience make it a widely used option.

Imatinib Eg Labo should be stored at temperatures below 25 °C, in the original container, protected from moisture and direct light. Do not store in bathrooms or near heat sources to maintain product stability.

The medication is taken orally, usually as a whole tablet swallowed with water. It can be taken with or without food, but patients should follow the prescriber’s instructions regarding timing and any dietary considerations.

Serious adverse events include severe neutropenia, hepatotoxicity, cardiac failure, pulmonary hypertension, and rare anaphylactic reactions. Patients should be monitored regularly for blood counts, liver function, and cardiac status, and any concerning symptoms reported promptly.

Imatinib is contraindicated in individuals with known hypersensitivity to the drug or any of its excipients. Caution is advised for patients with pre‑existing liver disease, cardiac dysfunction, or uncontrolled infections. The prescriber must evaluate each patient’s medical history before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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