Product image of Imatinib Accord (Imatinib) supplied by GNH India

Imatinib Accord

Active Ingredient:
Imatinib
Origin:
EU

Imatinib Accord (Imatinib)

Imatinib, the active ingredient in Imatinib Accord, is a tyrosine kinase inhibitor presented as an oral formulation for oral use. It is used to treat chronic myeloid leukemia and gastrointestinal stromal tumor in adult patients.
GNH India supplies Imatinib Accord as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Accord Healthcare S.L.U.

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Indications & Clinical Uses

Imatinib acts on malignant cells that depend on BCR‑ABL, c‑KIT or PDGFR signaling pathways.

  • Chronic myeloid leukemia (CML): provides disease control by inhibiting leukemic cell proliferation.
  • Gastrointestinal stromal tumor (GIST): reduces tumor growth and stabilises disease progression.
  • Philadelphia‑positive acute lymphoblastic leukemia (Ph+ ALL): achieves remission by targeting the same tyrosine‑kinase drivers.

How It Works

  • Imatinib selectively inhibits the ATP‑binding sites of BCR‑ABL, c‑KIT and platelet‑derived growth factor receptor (PDGFR) tyrosine kinases. By blocking these enzymes, it prevents downstream phosphorylation events that drive uncontrolled cell division, thereby suppressing malignant cell proliferation and inducing apoptosis in susceptible cancer cells.

Side Effects

Adverse reactions may occur with imatinib therapy.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Edema: swelling of the hands, feet or face.
  • Muscle cramps: occasional tightness or pain in muscles.
  • Fatigue: general tiredness or lack of energy.
  • Diarrhoea: loose stools occurring intermittently.
  • Rash: skin irritation or redness.

Serious or Rare Side Effects

  • Neutropenia: significant reduction in white blood cells, increasing infection risk.
  • Hepatotoxicity: elevated liver enzymes or liver injury.
  • Cardiac failure: signs of reduced heart function such as shortness of breath.
  • Severe fluid retention: rapid weight gain or pleural effusion.
  • Anaphylaxis: rare but potentially life‑threatening allergic reaction.

Precautions & Warnings

Patients receiving imatinib should be monitored for safety and efficacy.

  • Blood counts: regular CBC to detect neutropenia or thrombocytopenia.
  • Liver function: periodic tests for hepatotoxicity.
  • Cardiac assessment: evaluate for heart failure signs, especially in at‑risk individuals.
  • Hypersensitivity: discontinue if severe allergic reactions develop.
  • Renal impairment: adjust monitoring in patients with reduced kidney function.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Imatinib may interact with other medicines, altering its effectiveness or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): can raise imatinib plasma levels and increase toxicity.
  • Strong CYP3A4 inducers (e.g., rifampin, phenytoin): may lower imatinib concentrations, reducing therapeutic effect.

Moderate Interactions (Monitor Closely)

  • Proton‑pump inhibitors (e.g., omeprazole): may affect gastric pH and reduce absorption.
  • Warfarin: requires INR monitoring due to potential anticoagulant effect changes.
  • CYP2C8 inhibitors (e.g., gemfibrozil): can modestly increase imatinib exposure.
  • Vaccines (live attenuated): assess risk‑benefit before administration.

Frequently Asked Questions

Imatinib Accord is prescribed for chronic myeloid leukemia, gastrointestinal stromal tumor, and Philadelphia‑positive acute lymphoblastic leukemia. In each case the drug targets specific tyrosine‑kinase pathways that drive the growth of malignant cells, helping to control disease progression.

Imatinib blocks the ATP‑binding pockets of BCR‑ABL, c‑KIT and PDGFR tyrosine kinases. By preventing these enzymes from phosphorylating downstream proteins, the drug stops signals that promote uncontrolled cell division, leading to reduced tumor growth and, in many cases, cancer cell death.

The exact dose of Imatinib Accord is determined by the prescribing clinician based on the patient’s diagnosis, disease stage, weight, renal and hepatic function, and other individual factors. Healthcare providers set the regimen according to approved guidelines and patient‑specific considerations.

The safety of imatinib in pregnancy and lactation has not been established, and the product is classified as pregnancy category unknown. It should only be used if the potential benefit justifies the potential risk to the fetus or infant, and decisions are made in consultation with a specialist.

To place an order, submit an enquiry on the Imatinib Accord 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 was the first BCR‑ABL inhibitor and remains a standard of care for CML and GIST. Compared with newer agents, it has a well‑characterised safety profile and extensive clinical experience, though some newer inhibitors may offer activity against resistant mutations or different dosing schedules.

Imatinib Accord should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight and excessive heat to maintain stability and potency throughout its shelf life.

Imatinib Accord is taken orally, usually with a glass of water. The tablet should be swallowed whole and can be taken with or without food, unless the prescriber advises otherwise. Consistent daily dosing helps maintain steady drug levels.

Serious risks include severe neutropenia, hepatotoxicity, cardiac failure, and rare anaphylactic reactions. Patients should be monitored regularly for blood‑cell counts, liver enzymes and cardiac function, and any signs of infection, jaundice, shortness of breath or allergic response should prompt immediate medical evaluation.

Imatinib is contraindicated in individuals with known hypersensitivity to imatinib or any of its excipients. Caution is also advised for patients with severe hepatic impairment, uncontrolled cardiac disease, or those taking medications that strongly interact with its metabolism, unless a specialist determines the benefits outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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