GNH USA

Europe — EMA

Imatinib Teva

GNH USA supplies Imatinib Teva (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 Teva, is a tyrosine kinase inhibitor presented as a tablet for oral use. It is indicated for the treatment of chronic myeloid leukemia and gastrointestinal stromal tumor in adult patients.

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

What is Imatinib used for?

Imatinib Teva is a targeted antineoplastic agent that interferes with specific oncogenic signaling pathways.

- Chronic myeloid leukemia (CML): helps achieve hematologic and cytogenetic remission by suppressing malignant clone proliferation. - Gastrointestinal stromal tumor (GIST): reduces tumor growth and disease progression in patients with KIT or PDGFRA mutations. - Philadelphia‑positive acute lymphoblastic leukemia (Ph+ ALL): contributes to remission when used in combination regimens.

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 ankles. - Fatigue: generalized tiredness. - Diarrhea: loose stools. - Muscle cramps: occasional skeletal discomfort. - Rash: mild skin irritation.

Serious or Rare Side Effects: - Hepatotoxicity: elevated liver enzymes or liver injury. - Myelosuppression: neutropenia, anemia, or thrombocytopenia. - Cardiotoxicity: congestive heart failure signs. - Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis. - Pulmonary hypertension: shortness of breath and elevated pulmonary pressure. - Renal impairment: increased creatinine or reduced clearance.

What precautions apply to Imatinib?

Patients and prescribers should consider several safety measures before and during therapy.

- Baseline assessment: obtain complete blood count, liver function tests, and renal function before initiating treatment. - Monitoring: perform regular hematologic and biochemical labs to detect early toxicity. - Drug interactions: review concomitant medications for potential CYP3A4 modulators. - Pregnancy and lactation: avoid use unless benefits clearly outweigh potential risks. - Cardiovascular health: assess cardiac function in patients with pre‑existing heart disease. - Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture and direct sunlight.

What does Imatinib interact with?

Imatinib may alter the pharmacokinetics of several co‑administered agents.

Major Interactions (Avoid): - Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may markedly reduce imatinib exposure. - Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): can increase plasma levels and toxicity risk.

Moderate Interactions (Monitor Closely): - Acid‑reducing agents (e.g., proton pump inhibitors, antacids): may affect absorption, consider timing adjustments. - Anticoagulants (e.g., warfarin): monitor INR more frequently. - Vaccines: live attenuated vaccines should be avoided during therapy. - Concomitant chemotherapy: assess overlapping toxicities, especially myelosuppression.

Frequently asked questions

What conditions is Imatinib Teva used to treat?+
Imatinib Teva is prescribed for chronic myeloid leukemia (CML), gastrointestinal stromal tumor (GIST) with KIT or PDGFRA mutations, and Philadelphia‑positive acute lymphoblastic leukemia when used in combination therapy. It targets the underlying molecular drivers of these cancers.
How does Imatinib work at the molecular level?+
Imatinib binds to the ATP‑binding site of BCR‑ABL, KIT, and PDGFRA tyrosine kinases, preventing their activation. This blocks downstream signaling pathways that promote malignant cell proliferation and survival, leading to apoptosis of cancerous cells.
What is the typical dosing regimen for Imatinib Teva?+
The exact dose and schedule are determined by the prescribing clinician based on the specific indication, disease stage, patient weight, and renal or hepatic function. Patients should follow the individualized prescription provided by their healthcare professional.
Is Imatinib safe to use during pregnancy or breastfeeding?+
Imatinib is classified as contraindicated or used with caution during pregnancy and lactation because animal studies have shown fetal risk and it can be excreted in breast milk. Women of child‑bearing potential should discuss contraception and risk‑benefit considerations with their physician.
How do I order Imatinib Teva 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 needs), and required import documentation.
How does Imatinib compare with other tyrosine kinase inhibitors?+
Imatinib was the first BCR‑ABL inhibitor and remains a standard of care for CML and GIST. Newer agents such as dasatinib or nilotinib may offer potency advantages in resistant disease, but Imatinib’s long‑term safety profile and extensive clinical experience make it a widely used first‑line option.
What are the recommended storage conditions for Imatinib Teva?+
Store the tablets at ambient temperature, preferably below 25 °C. Keep them in the original container, protect from moisture, heat, and direct sunlight to maintain product stability throughout its shelf life.
How is Imatinib Teva administered to patients?+
Imatinib Teva is taken orally, usually once daily, with or without food. The tablet should be swallowed whole with a glass of water. Patients should not crush or chew the tablet unless specifically instructed by a healthcare professional.
What are the most serious risks associated with Imatinib therapy?+
Serious adverse events include hepatotoxicity, severe myelosuppression (neutropenia, anemia, thrombocytopenia), cardiac failure, pulmonary hypertension, and rare but life‑threatening skin reactions such as Stevens‑Johnson syndrome. Prompt medical evaluation is required if any of these symptoms appear.
Who should not take Imatinib Teva?+
Patients with known hypersensitivity to imatinib or any of its excipients should avoid the drug. Those with uncontrolled cardiac disease, severe hepatic impairment, or who are pregnant without a clear therapeutic justification should not use Imatinib unless a specialist determines that benefits outweigh risks.
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
Teva B.V
Origin
EU

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