Product image of Imanivec (Imatinib) supplied by GNH India

Imanivec

Active Ingredient:
Imatinib
Origin:
EU

Imanivec (Imatinib)

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

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

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

Imanivec (imatinib) is a tyrosine kinase inhibitor used in malignancies driven by specific kinase mutations.

  • Chronic myeloid leukemia: reduces disease burden and improves survival by targeting BCR‑ABL‑positive cells.
  • Philadelphia‑positive acute lymphoblastic leukemia: induces remission by inhibiting BCR‑ABL signaling.
  • Gastrointestinal stromal tumor: controls tumor growth by blocking c‑KIT and PDGFR activity.

How It Works

  • Imatinib binds to the ATP‑binding pocket of BCR‑ABL, c‑KIT and PDGFR tyrosine kinases, stabilising them in an inactive conformation. This blocks downstream phosphorylation cascades that drive uncontrolled cell proliferation, thereby inducing apoptosis or growth arrest in malignant cells that depend on these kinases for survival.

Side Effects

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

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Edema: swelling of the hands, feet, or face.
  • Fatigue: persistent tiredness.
  • Muscle cramps: painful tightening of muscles.
  • Diarrhoea: loose stools.
  • Rash: skin irritation or redness.

Serious or Rare Side Effects

  • Neutropenia: dangerously low white‑blood‑cell count.
  • Thrombocytopenia: reduced platelet levels leading to bleeding risk.
  • Hepatotoxicity: liver enzyme elevation or injury.
  • Cardiac failure: signs of reduced heart function.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Pulmonary hypertension: elevated pressure in lung arteries.

Precautions & Warnings

Before initiating therapy, clinicians should assess baseline health status and monitor for potential complications.

  • Monitor blood counts: perform regular CBC to detect cytopenias.
  • Assess liver function: check hepatic enzymes periodically.
  • Evaluate cardiac status: consider ECG or echocardiogram in patients with heart disease.
  • Review concomitant medications: avoid drugs that strongly affect CYP3A4 metabolism.
  • Pregnancy and lactation: discuss risks with women of childbearing potential.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may raise imatinib levels.
  • Strong CYP3A4 inducers (e.g., rifampin, phenytoin): may reduce efficacy.
  • QT‑prolonging agents (e.g., sotalol, quinidine): increase risk of cardiac arrhythmia.

Moderate Interactions (Monitor Closely)

  • Warfarin: may enhance anticoagulant effect, monitor INR.
  • Oral contraceptives: possible reduced hormonal efficacy.
  • H2‑blockers or antacids: may affect absorption, separate dosing times.
  • CYP2C8 inhibitors (e.g., gemfibrozil): modest increase in exposure.
  • Proton‑pump inhibitors: monitor for altered gastric pH affecting drug uptake.

Frequently Asked Questions

Imanivec (imatinib) is prescribed for chronic myeloid leukemia, Philadelphia‑positive acute lymphoblastic leukemia, and gastrointestinal stromal tumor. In each case the drug targets specific tyrosine kinases that drive malignant cell growth, helping to control disease progression and improve patient outcomes.

Imatinib binds to the ATP‑binding site of BCR‑ABL, c‑KIT and PDGFR tyrosine kinases, locking them in an inactive shape. This blocks downstream signaling pathways that promote cell division and survival, leading to reduced proliferation of cancer cells that rely on these kinases.

The dosage of Imanivec is individualized by the treating physician based on the specific indication, disease stage, patient weight, renal and hepatic function, and other clinical factors. Only a qualified healthcare professional should determine the appropriate dose and schedule.

Safety data for imatinib in pregnancy and lactation are limited. The drug may pose risks to the developing fetus and can be excreted in breast milk. Women who are pregnant, planning pregnancy, or breastfeeding should discuss potential benefits and risks with their oncologist before starting therapy.

To request Imanivec, submit an enquiry on the product page at gnhindia.com with 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 (including any cold‑chain needs) and necessary import documentation.

Imatinib was the first BCR‑ABL inhibitor and remains a standard of care for its approved indications. Compared with newer agents, it has a well‑characterised safety profile and extensive clinical experience, though some newer inhibitors may offer activity against resistant mutations or different dosing conveniences.

Imanivec tablets should be stored at ambient temperature, preferably below 25 °C. Keep the product in its original container, protect it from moisture and direct light, and avoid storing in areas with high humidity or temperature fluctuations.

Imanivec is taken orally, usually once daily, with or without food as directed by the prescribing clinician. Tablets should be swallowed whole with a glass of water and not crushed or chewed unless specifically instructed.

Serious adverse events include severe neutropenia, thrombocytopenia, hepatotoxicity, cardiac failure, pulmonary hypertension, and rare but life‑threatening skin reactions such as Stevens‑Johnson syndrome. Patients should be monitored regularly for these complications, and any concerning symptoms should be reported promptly.

Patients with known hypersensitivity to imatinib or any of its excipients should avoid the drug. Caution is also advised for individuals with uncontrolled infections, severe hepatic impairment, or significant cardiac disease, and the medication should be used only under close medical supervision in these cases.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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