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 certain blood cancers and solid tumours that depend on BCR‑ABL, c‑KIT or PDGFR signaling.
GNH India supplies Imatinib Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

Imatinib targets malignant cells driven by specific tyrosine‑kinase pathways and is used in several approved oncologic indications.

  • Chronic myeloid leukemia (CML): reduces proliferation of BCR‑ABL‑positive leukemic cells and improves long‑term survival.
  • Gastrointestinal stromal tumor (GIST): blocks c‑KIT‑driven tumor growth and helps achieve disease control.
  • Philadelphia chromosome‑positive acute lymphoblastic leukemia (Ph+ ALL): provides targeted inhibition of BCR‑ABL to achieve remission in eligible patients.

How It Works

  • Imatinib binds competitively to the ATP‑binding pocket of BCR‑ABL, c‑KIT and PDGFR tyrosine kinases, preventing phosphorylation of downstream substrates. This inhibition halts proliferative signaling cascades, induces apoptosis of malignant cells, and limits angiogenesis, thereby controlling tumour growth in responsive cancers.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Nausea and vomiting
  • Peripheral edema
  • Muscle cramps or pain
  • Fatigue
  • Diarrhoea
  • Skin rash

Serious or Rare Side Effects

  • Neutropenia or severe leukopenia
  • Hepatotoxicity with elevated transaminases
  • Cardiac failure or reduced left‑ventricular function
  • Pulmonary arterial hypertension
  • Anaphylaxis or severe hypersensitivity reactions

Precautions & Warnings

Patients should be monitored closely for laboratory and clinical changes that may require dose adjustment or temporary discontinuation.

  • Blood counts: monitor complete blood count regularly to detect cytopenias.
  • Liver function: assess hepatic enzymes before initiation and periodically during therapy.
  • Cardiac health: avoid in patients with pre‑existing severe heart failure.
  • Renal function: use caution and adjust dose in moderate to severe renal impairment.
  • Pregnancy and lactation: safety not established; discuss risks with a healthcare professional.
  • Store at room temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Imatinib may interact with other medicines that affect its metabolism or pharmacodynamic profile.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase imatinib exposure and toxicity.
  • Strong CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce efficacy by lowering plasma levels.
  • Concomitant use with potent P‑glycoprotein inhibitors can raise systemic concentrations.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., fluconazole, erythromycin): may require dose adjustment.
  • Anticoagulants such as warfarin: imatinib can alter INR, necessitating closer monitoring.
  • Diuretics (e.g., furosemide): may exacerbate fluid retention; monitor for edema.

Frequently Asked Questions

Imatinib Stada is indicated for chronic myeloid leukemia, gastrointestinal stromal tumour, and Philadelphia chromosome‑positive acute lymphoblastic leukaemia. In each case the drug targets specific tyrosine‑kinase abnormalities that drive malignant cell growth, helping to achieve disease control and improve survival when used as part of an approved treatment regimen.

Imatinib blocks the ATP‑binding sites of BCR‑ABL, c‑KIT and PDGFR tyrosine kinases. By preventing these enzymes from phosphorylating downstream proteins, the drug stops the signalling pathways that promote cell division, survival and angiogenesis, leading to reduced tumour proliferation and increased cancer cell death.

The exact dose of Imatinib Stada is determined by the prescribing clinician based on the patient’s diagnosis, disease stage, body weight, renal and hepatic function, and any concomitant therapies. Healthcare professionals follow approved dosing guidelines and may adjust the regimen according to therapeutic response and tolerability.

Safety data for Imatinib Stada in pregnancy and lactation are limited. The drug may pose risks to the developing fetus and to a nursing infant. Women who are pregnant, planning to become pregnant, or breastfeeding should discuss potential benefits and risks with their treating physician before using the medication.

To request Imatinib Stada, 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 (including any cold‑chain requirements) and the necessary import documentation.

Imatinib was the first BCR‑ABL inhibitor and remains a standard of care for several indications. 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. Choice of therapy depends on disease characteristics, mutation status, prior treatment history and physician judgment.

Imatinib Stada should be stored at room temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the product away from excessive heat and humidity, and do not store in the bathroom or near a kitchen sink.

Imatinib Stada is taken orally, usually with a glass of water. It can be swallowed with or without food, but patients should follow any specific instructions from their healthcare provider. The tablet should not be crushed or chewed unless the prescriber advises otherwise.

Serious risks include severe neutropenia or other cytopenias, hepatotoxicity with marked liver enzyme elevation, cardiac failure or reduced left‑ventricular function, pulmonary arterial hypertension, and life‑threatening allergic reactions such as anaphylaxis. Patients should be monitored regularly for these events and report any concerning symptoms promptly.

Imatinib Stada is contraindicated in patients with known hypersensitivity to imatinib or any of its excipients. Caution is advised for individuals with severe cardiac disease, uncontrolled infections, or significant hepatic impairment. The drug should also be avoided in patients for whom the benefits do not outweigh the potential risks, as determined by a qualified clinician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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