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

Imatinib Beta

Active Ingredient:
Imatinib
Origin:
EU

Imatinib Beta (Imatinib)

Imatinib, the active ingredient in Imatinib Beta, is a tyrosine kinase inhibitor presented as an unspecified strength/oral tablet for oral use. It targets specific cancers such as chronic myeloid leukemia, gastrointestinal stromal tumor, and Philadelphia chromosome‑positive acute lymphoblastic leukemia in adult patients.

GNH India supplies Imatinib Beta as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide. The company adheres to EU quality standards and provides regulatory documentation for global distribution.

Manufacturer / TM Owner

Betapharm Arzneimittel Gmbh

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Indications & Clinical Uses

Imatinib Beta is used to treat malignancies driven by abnormal tyrosine‑kinase signaling.

  • Chronic myeloid leukemia (CML): reduces leukemic cell proliferation and improves survival.
  • Gastrointestinal stromal tumor (GIST): inhibits tumor growth driven by c‑KIT mutations.
  • Philadelphia chromosome‑positive acute lymphoblastic leukemia (Ph+ ALL): blocks BCR‑ABL activity to achieve remission.

How It Works

  • Imatinib selectively binds to the ATP‑binding pocket of BCR‑ABL, c‑KIT and platelet‑derived growth factor receptors (PDGFR), inhibiting their tyrosine‑kinase activity. This blockade prevents downstream signaling that drives uncontrolled cell division, survival and migration, leading to apoptosis of malignant cells while sparing most normal tissues.

Side Effects

Imatinib Beta may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Edema: swelling of the hands, feet or ankles.
  • Muscle cramps: intermittent tightness or pain in skeletal muscles.
  • Fatigue: generalized tiredness affecting daily activities.

Serious or Rare Side Effects

  • Severe neutropenia: marked reduction in white blood cells, increasing infection risk.
  • Hepatotoxicity: elevated liver enzymes or liver injury requiring monitoring.
  • Cardiac failure: signs of reduced heart function such as shortness of breath or peripheral edema.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific factors and monitor for potential complications.

  • Dose adjustment in renal impairment: assess renal function and consider reduced dosing.
  • Monitor hepatic function: check liver enzymes regularly during treatment.
  • Assess for cardiovascular disease: watch for signs of heart failure or reduced ejection fraction.
  • Avoid in patients with known hypersensitivity to imatinib or its excipients.
  • Pregnancy and lactation: use only if the potential benefit justifies the risk to the fetus or infant.
  • Store at ambient temperature below 25°C: keep in the original pack, protect from moisture and light.

Avoid Interactions

Imatinib interacts with several medicines that can alter its plasma concentration or increase toxicity.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin): may markedly reduce imatinib exposure.
  • Antacids containing aluminum or magnesium: can decrease oral absorption of imatinib.
  • Concurrent use with other BCR‑ABL inhibitors: increases risk of overlapping toxicities.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may raise imatinib levels and require dose adjustment.
  • Warfarin: imatinib can enhance anticoagulant effect; monitor INR closely.

Frequently Asked Questions

Imatinib Beta is indicated for the treatment of chronic myeloid leukemia, gastrointestinal stromal tumor, and Philadelphia chromosome‑positive acute lymphoblastic leukemia. It works by targeting the abnormal tyrosine‑kinase activity that drives these cancers.

Imatinib binds to the ATP‑binding site of BCR‑ABL, c‑KIT and PDGFR tyrosine kinases, blocking their enzymatic activity. This inhibition stops downstream signaling pathways that promote uncontrolled cell growth, leading to cancer cell death while sparing most normal cells.

The specific dose of Imatinib Beta is determined by the prescribing clinician based on the patient’s diagnosis, disease stage, body weight, renal and hepatic function, and other individual factors. No fixed dosing information is provided here.

Safety data for Imatinib in pregnancy and lactation are limited. It should only be used if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and this decision must be made by the treating physician.

To place an order, submit an enquiry on the Imatinib Beta 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 approved and remains a standard of care for CML and Ph+ ALL. Newer agents such as dasatinib or nilotinib may offer potency advantages or activity against certain resistant mutations, but choice of therapy depends on disease characteristics, prior treatment history and individual patient factors.

Imatinib Beta should be stored at ambient temperature below 25 °C. Keep the product in its original packaging, protect it from moisture and direct sunlight, and discard any tablets that appear discoloured or damaged.

Imatinib Beta is taken orally, usually with a glass of water. It can be taken with or without food, but patients should follow the specific instructions provided by their healthcare professional to maintain consistent absorption.

Serious risks include severe neutropenia, hepatotoxicity and cardiac failure. Patients should be monitored regularly for signs of infection, liver enzyme elevations and heart function changes, and any concerning symptoms should be reported to a healthcare provider promptly.

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 who are pregnant unless the benefits outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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