GNH USA

Europe — EMA

Imatinib Krka D.D.

GNH USA supplies Imatinib Krka D.D. (Imatinib), a tyrosine kinase inhibitor for chronic myeloid leukemia, Ph+ ALL and GIST. Request a quote for global supply.

Imatinib

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What is Imatinib?

Imatinib, the active ingredient in Imatinib Krka D.D., is a tyrosine kinase inhibitor presented as an oral tablet for oral use. It is employed in the treatment of chronic myeloid leukemia, Philadelphia chromosome‑positive acute lymphoblastic leukemia and gastrointestinal stromal tumours in adult patients.

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

What is Imatinib used for?

Imatinib acts on malignant cells driven by BCR‑ABL, c‑KIT or PDGFR signaling pathways, providing targeted therapy for specific hematologic and solid tumours. - Chronic myeloid leukemia (CML): achieves disease control by inhibiting BCR‑ABL‑driven proliferation. - Philadelphia chromosome‑positive acute lymphoblastic leukemia (Ph+ ALL): facilitates remission through BCR‑ABL blockade. - Gastrointestinal stromal tumour (GIST): induces tumour shrinkage by targeting c‑KIT and PDGFR signaling.

What are the side effects of Imatinib?

Adverse reactions may vary in frequency and severity. Patients should be monitored regularly for any new or worsening symptoms.

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

Serious or Rare Side Effects: - Hepatotoxicity: elevated liver enzymes or liver injury. - Cardiac dysfunction: reduced left‑ventricular ejection fraction. - Severe neutropenia or thrombocytopenia: increased risk of infection or bleeding.

What precautions apply to Imatinib?

Before initiating therapy, clinicians should assess baseline organ function and comorbid conditions. - 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 for CYP3A4 inhibitors or inducers. - Pregnancy and lactation: avoid use unless benefits clearly outweigh potential risks. - Store at ambient temperature: keep below 25 °C in the original container, protect from moisture and direct sunlight.

What does Imatinib interact with?

Imatinib may interact with several medicines that alter its metabolism or increase toxicity. Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may raise imatinib plasma levels. - Potent CYP3A4 inducers (e.g., rifampicin, carbamazepine): may reduce therapeutic exposure. Moderate Interactions (Monitor Closely): - Acid‑reducing agents (e.g., proton pump inhibitors): can modestly decrease absorption. - Anticoagulants (e.g., warfarin): may enhance bleeding risk. - Vaccines containing live attenuated virus: consider timing to avoid reduced efficacy.

Frequently asked questions

What conditions is Imatinib Krka D.D. used to treat?+
Imatinib Krka D.D. is indicated for chronic myeloid leukemia, Philadelphia chromosome‑positive acute lymphoblastic leukemia, and gastrointestinal stromal tumours. In each case the drug targets specific tyrosine kinases that drive malignant cell growth, helping to control disease progression.
How does imatinib work at the molecular level?+
Imatinib binds to the ATP‑binding pocket of BCR‑ABL, c‑KIT and PDGFR tyrosine kinases, blocking their activity. This inhibition stops downstream signaling that promotes cell division, leading to reduced proliferation of cancer cells and, in many cases, induction of apoptosis.
What is the usual dose of Imatinib Krka D.D.?+
The specific dose and dosing schedule are determined by the prescribing clinician based on the patient’s diagnosis, disease stage, renal and hepatic function, and other individual factors. Healthcare professionals tailor the regimen to achieve optimal therapeutic effect while minimizing risk.
Is Imatinib Krka D.D. safe during pregnancy or breastfeeding?+
Safety data in pregnancy and lactation are limited. The drug should only be used if the potential benefit justifies the potential risk to the fetus or infant. Women of child‑bearing potential should discuss contraception and treatment options with their healthcare provider.
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 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.
What are the recommended storage conditions for Imatinib Krka D.D.?+
Store the tablets at ambient temperature, preferably below 25 °C. Keep them in the original blister or container, protect from moisture, heat and direct sunlight, and ensure the packaging remains tightly closed until use.
How is Imatinib Krka D.D. administered?+
Imatinib Krka D.D. is taken orally, usually with a glass of water. It can be swallowed with or without food, but patients should follow the prescribing physician’s instructions regarding timing relative to meals to maintain consistent absorption.
What are the most serious risks associated with Imatinib therapy?+
Serious adverse events include hepatotoxicity, severe neutropenia or thrombocytopenia, and cardiac dysfunction such as reduced left‑ventricular ejection fraction. Patients should be monitored regularly for liver enzymes, blood counts and cardiac function, and any concerning symptoms reported promptly.
Who should not use Imatinib Krka D.D.?+
Patients with known hypersensitivity to imatinib or any of its excipients should avoid the product. Caution is also advised for individuals with severe hepatic impairment, uncontrolled cardiac disease, or those taking contraindicated strong CYP3A4 inhibitors or inducers without medical supervision.
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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