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

Imatinib Stada

Active Ingredient:
Imatinib
Origin:
EU

Imatinib Stada (Imatinib)

Imatinib, the active ingredient in Imatinib Stada, is a tyrosine kinase inhibitor presented as an oral formulation for oral use. It is employed in the treatment of several BCR‑ABL positive cancers, including chronic myeloid leukemia, Philadelphia chromosome‑positive acute lymphoblastic leukemia and gastrointestinal stromal tumor.
GNH India supplies Imatinib Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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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): suppresses leukemic cell proliferation and induces remission.
  • Philadelphia chromosome‑positive acute lymphoblastic leukemia (Ph+ ALL): improves survival by targeting the BCR‑ABL fusion protein.
  • Gastrointestinal stromal tumor (GIST): inhibits c‑KIT driven tumor growth.
  • Other BCR‑ABL positive hematologic malignancies: provides disease control where BCR‑ABL drives pathology.

How It Works

  • Imatinib selectively inhibits the ATP‑binding site of BCR‑ABL tyrosine kinase as well as the related kinases c‑KIT and platelet‑derived growth factor receptor (PDGFR). By blocking these enzymes, it prevents downstream phosphorylation events that drive uncontrolled cell division, thereby reducing proliferation of malignant cells and promoting apoptosis in susceptible tumor populations.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Nausea: mild to moderate gastrointestinal upset.
  • Edema: peripheral swelling, often of the hands or feet.
  • Fatigue: generalized tiredness.
  • Diarrhea: loose stools, usually self‑limiting.
  • Muscle cramps: intermittent skeletal muscle discomfort.

Serious or Rare Side Effects

  • Hepatotoxicity: elevated liver enzymes or jaundice.
  • Cardiotoxicity: decreased left‑ventricular ejection fraction.
  • Severe neutropenia: markedly reduced white‑blood cell count increasing infection risk.

Precautions & Warnings

Before initiating therapy, clinicians should assess baseline organ function and monitor throughout treatment.

  • Baseline labs: obtain complete blood count, liver and renal function tests.
  • Cardiac monitoring: evaluate ejection fraction in patients with pre‑existing heart disease.
  • Drug interactions: review concomitant medications that affect CYP3A4 metabolism.
  • Pregnancy and lactation: avoid use unless benefits outweigh potential risks.
  • Patient counseling: advise on signs of infection, bleeding, or liver dysfunction.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Imatinib may interact with several agents that alter its plasma concentration or pharmacodynamic profile.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may markedly reduce efficacy.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): can increase toxicity risk.

Moderate Interactions (Monitor Closely)

  • Acid‑suppressing agents (e.g., proton pump inhibitors, antacids): may affect absorption.
  • Concomitant anticoagulants (e.g., warfarin): monitor INR for potential bleeding.
  • Vaccines: live attenuated vaccines should be avoided during treatment.

Frequently Asked Questions

Imatinib Stada is prescribed for cancers that rely on BCR‑ABL, c‑KIT or PDGFR signaling, including chronic myeloid leukemia, Philadelphia chromosome‑positive acute lymphoblastic leukemia, gastrointestinal stromal tumor, and other BCR‑ABL positive hematologic malignancies.

Imatinib binds to the ATP‑binding pocket of BCR‑ABL, c‑KIT and PDGFR tyrosine kinases, blocking their activity. This inhibition stops downstream phosphorylation cascades that drive uncontrolled cell growth, leading to reduced tumor proliferation and increased cancer cell death.

The specific dose of Imatinib Stada is determined by the prescribing physician based on the patient’s diagnosis, disease stage, renal and hepatic function, and other clinical factors. Dosage regimens are individualized and should follow the prescriber’s instructions.

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

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 was the first BCR‑ABL tyrosine kinase inhibitor approved for chronic myeloid leukemia and remains a standard first‑line option. Newer agents such as dasatinib or nilotinib may be used when resistance or intolerance to Imatinib occurs, but Imatinib’s long‑term safety profile and extensive clinical experience make it a widely accepted choice.

Imatinib Stada should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the product from moisture, excessive heat and direct sunlight to maintain its stability and potency.

Imatinib Stada 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 unless specifically instructed.

Serious adverse events include hepatotoxicity, severe neutropenia, and cardiotoxicity such as reduced left‑ventricular ejection fraction. Patients should be monitored regularly for liver function abnormalities, blood count changes, and cardiac function throughout therapy.

Imatinib Stada is contraindicated in patients with known hypersensitivity to imatinib or any of its excipients. Caution is also advised for individuals with severe hepatic impairment, uncontrolled heart failure, or those taking strong CYP3A4 inducers or inhibitors without appropriate monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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