GNH USA

Europe — EMA

Imatinib Krka D.D.

GNH USA supplies Imatinib Krka D.D. (Imatinib), a tyrosine kinase inhibitor for chronic myeloid leukemia and gastrointestinal stromal tumor.

Imatinib

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What is Imatinib?

Imatinib, the active ingredient in Imatinib Krka D.D., is a tyrosine kinase inhibitor presented as a strength/form for oral use. It treats chronic myeloid leukemia and gastrointestinal stromal tumor in adult patients.

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

What is Imatinib used for?

Imatinib acts on BCR‑ABL driven malignancies and related tyrosine‑kinase pathways. - Chronic myeloid leukemia (CML): restores normal blood cell production and reduces disease burden. - Gastrointestinal stromal tumor (GIST): blocks KIT signaling to inhibit tumor growth. - Philadelphia chromosome‑positive acute lymphoblastic leukemia (Ph+ ALL): contributes to remission when combined with chemotherapy.

What are the side effects of Imatinib?

Adverse reactions may vary in frequency and severity.

Common Side Effects: - Nausea: mild to moderate gastrointestinal upset. - Edema: peripheral swelling, often in the lower extremities. - Fatigue: persistent tiredness affecting daily activities. - Diarrhea: loose stools that may require hydration.

Serious or Rare Side Effects: - Neutropenia: marked reduction in white blood cells increasing infection risk. - Hepatotoxicity: elevated liver enzymes or liver injury. - Cardiac failure: signs of reduced cardiac output, especially in patients with pre‑existing heart disease. - Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis. - Pulmonary hypertension: elevated pressure in lung arteries presenting with dyspnea.

What precautions apply to Imatinib?

Patients should be monitored closely for safety concerns before and during therapy. - Blood count monitoring: perform complete blood counts regularly to detect cytopenias. - Liver function assessment: check hepatic enzymes at baseline and periodically. - Cardiac evaluation: assess cardiac history and monitor for signs of heart failure. - Hypersensitivity avoidance: discontinue if severe allergic reactions occur. - Pregnancy and lactation counseling: discuss potential risks with a healthcare professional. - Store at below 25°C: keep in the original container, protect from moisture and direct sunlight.

What does Imatinib interact with?

Imatinib may interact with several co‑administered medicines.

Major Interactions (Avoid): - CYP3A4 strong inhibitors (e.g., ketoconazole, clarithromycin): can raise imatinib plasma levels. - CYP3A4 strong inducers (e.g., rifampicin, carbamazepine): may reduce efficacy. - Acid‑reducing agents (e.g., high‑dose PPIs): can lower absorption.

Moderate Interactions (Monitor Closely): - Anticoagulants (e.g., warfarin): may increase bleeding risk; monitor INR. - Vaccines (live attenuated): consider timing to avoid reduced vaccine efficacy.

Frequently asked questions

What conditions is Imatinib Krka D.D. used to treat?+
Imatinib Krka D.D. is prescribed for chronic myeloid leukemia, gastrointestinal stromal tumor, and Philadelphia chromosome‑positive acute lymphoblastic leukemia. In each case, the drug targets abnormal tyrosine‑kinase activity that drives malignant cell growth, helping to achieve disease control and improve survival.
How does imatinib work at the molecular level?+
Imatinib binds to the ATP‑binding site of BCR‑ABL, KIT and PDGFR tyrosine kinases, blocking their enzymatic activity. This inhibition stops downstream phosphorylation events that normally promote cell proliferation and survival, thereby reducing the growth of cancer cells that depend on these pathways.
What is the usual dose of Imatinib Krka D.D.?+
The exact dose and dosing schedule are determined by the prescribing physician based on the specific indication, disease stage, patient weight, renal and hepatic function, and other clinical factors. Patients should follow the individualized regimen provided by their healthcare professional.
Is Imatinib Krka D.D. safe during pregnancy or breastfeeding?+
Safety data for imatinib in pregnancy and lactation are limited. It is generally advised that women of child‑bearing potential discuss potential risks with their physician, and that breastfeeding be avoided unless the benefits outweigh the possible risks to the infant.
How do I order Imatinib Krka D.D. 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 and any necessary import documentation.
How does Imatinib compare with other treatments for CML?+
Imatinib was the first BCR‑ABL tyrosine‑kinase inhibitor approved for CML and remains a standard first‑line option. Newer agents such as dasatinib and nilotinib have different potency and side‑effect profiles, but imatinib’s long‑term safety record and extensive clinical experience make it a widely used reference therapy.
What are the recommended storage conditions for Imatinib Krka D.D.?+
Store the product at temperatures below 25 °C in its original packaging. Protect it from moisture, excessive heat and direct sunlight to maintain stability and potency throughout its shelf life.
How is Imatinib Krka D.D. administered?+
Imatinib Krka D.D. is taken orally, usually as a whole tablet swallowed with water. It can be taken with or without food, but patients should follow any specific instructions from their prescriber regarding timing relative to meals.
What are the most serious risks associated with Imatinib therapy?+
Serious risks include severe neutropenia, hepatotoxicity, cardiac failure, pulmonary hypertension, and rare but life‑threatening skin reactions such as Stevens‑Johnson syndrome. Patients should be monitored regularly for these events and report any concerning symptoms promptly.
Who should not use Imatinib Krka D.D.?+
Patients with known hypersensitivity to imatinib or any of its excipients should avoid the drug. Caution is also advised for individuals with pre‑existing severe liver disease, uncontrolled cardiac conditions, or those taking medications that strongly interact with imatinib metabolism.
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
Krka, D.D., Novo Mesto
Origin
EU

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