GNH USA

Europe — EMA

Imatinib Devatis

GNH USA supplies Imatinib Devatis (Imatinib), a tyrosine kinase inhibitor for chronic myeloid leukemia, Philadelphia chromosome‑positive acute lymphoblastic

Imatinib

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What is Imatinib?

Imatinib, the active ingredient in Imatinib Devatis, is a tyrosine kinase inhibitor presented as an oral tablet for oral use. It treats chronic myeloid leukemia, Philadelphia chromosome‑positive acute lymphoblastic leukemia and gastrointestinal stromal tumor in adult patients.

GNH USA supplies Imatinib Devatis as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

What is Imatinib used for?

Imatinib is a targeted antineoplastic agent that acts on specific tyrosine‑kinase driven malignancies. - Chronic myeloid leukemia: suppresses BCR‑ABL driven proliferation, leading to hematologic and cytogenetic remission. - Philadelphia chromosome‑positive acute lymphoblastic leukemia: blocks leukemic cell growth and improves remission rates. - Gastrointestinal stromal tumor: inhibits c‑KIT and PDGFR signaling, reducing tumor size and disease progression.

What are the side effects of Imatinib?

Imatinib may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects: - Nausea: mild to moderate upset stomach. - Edema: peripheral swelling, especially in the ankles. - Muscle cramps: intermittent tightness or pain. - Fatigue: persistent tiredness. - Diarrhea: loose stools. - Rash: mild skin eruption.

Serious or Rare Side Effects: - Hepatotoxicity: elevated liver enzymes or jaundice. - Cardiotoxicity: reduced left‑ventricular ejection fraction. - Severe neutropenia: markedly low white‑blood‑cell count. - Hemorrhage: bleeding tendencies. - Pulmonary arterial hypertension: increased pressure in lung arteries. - Anaphylaxis: rare severe allergic reaction.

What precautions apply to Imatinib?

Before initiating therapy, clinicians should assess baseline organ function and monitor patients regularly. - Baseline labs: obtain CBC, liver and renal function tests. - Cardiac monitoring: evaluate ejection fraction in patients with cardiac risk. - Drug interactions: review concomitant medications for CYP3A4 inhibitors/inducers. - Pregnancy: avoid use unless benefits outweigh potential fetal risk. - Breastfeeding: contraindicated; advise against nursing while on therapy. - Store at ambient temperature: keep below 25 °C, retain in original container, protect from moisture and direct sunlight.

What does Imatinib interact with?

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

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may raise imatinib levels and risk toxicity. - Strong CYP3A4 inducers (e.g., rifampicin, carbamazepine): may lower efficacy by reducing drug exposure.

Moderate Interactions (Monitor Closely): - Acid‑reducing agents (e.g., proton pump inhibitors, antacids): can affect absorption; separate dosing by at least 2 hours. - Anticoagulants (e.g., warfarin): may increase bleeding risk; monitor INR. - Vaccines (live attenuated): potential reduced immune response; consider timing.

Frequently asked questions

What conditions is Imatinib Devatis used to treat?+
Imatinib Devatis is indicated for chronic myeloid leukemia, Philadelphia chromosome‑positive acute lymphoblastic leukemia, and gastrointestinal stromal tumor. In each case the drug targets specific tyrosine‑kinase pathways that drive malignant cell growth, helping to achieve disease control and improve survival outcomes.
How does imatinib work at the molecular level?+
Imatinib blocks the ATP‑binding sites of BCR‑ABL, c‑KIT and PDGFR tyrosine kinases. By preventing phosphorylation of downstream signaling proteins, it stops proliferative signals, induces apoptosis of cancer cells, and reduces tumor angiogenesis, which collectively suppresses disease progression.
What is the usual dose of Imatinib Devatis?+
The specific dose of Imatinib Devatis is determined by the prescribing clinician based on the patient’s diagnosis, disease stage, renal and hepatic function, and other individual factors. Healthcare professionals adjust the regimen to achieve optimal therapeutic effect while minimizing risk.
Is Imatinib Devatis safe during pregnancy or breastfeeding?+
The safety of Imatinib Devatis in pregnancy and lactation has not been established. It is generally advised to avoid use during pregnancy unless the potential benefit justifies the risk, and breastfeeding is contraindicated because the drug can be excreted in breast milk.
How do I order Imatinib Devatis from GNH USA?+
To place an order, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA 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 necessary import documentation.
How does Imatinib compare with other treatments for CML?+
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 and nilotinib offer alternative potency and side‑effect profiles, but imatinib’s long‑term safety data and cost‑effectiveness make it a widely used reference therapy.
What are the recommended storage conditions for Imatinib Devatis?+
Imatinib Devatis should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the product from moisture, direct sunlight, and excessive heat to maintain stability throughout its shelf life.
How is Imatinib Devatis administered to patients?+
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 prescribing clinician’s instructions regarding timing and any necessary dietary considerations.
What are the most serious risks associated with Imatinib Devatis?+
Serious adverse events include hepatotoxicity, severe neutropenia, cardiac dysfunction such as reduced left‑ventricular ejection fraction, pulmonary arterial hypertension, and rare anaphylactic reactions. Patients should be monitored regularly for these complications, and any concerning symptoms reported promptly.
Who should not use Imatinib Devatis?+
Imatinib Devatis 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 cardiac disease, or those who are pregnant or breastfeeding without a clear benefit outweighing the risk.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Imatinib
Route
Oral Use
Manufacturer
Devatis Gmbh
Origin
EU

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