Product image of Nilotinib Teva Uk (Nilotinib) supplied by GNH India

Nilotinib Teva Uk

Active Ingredient:
Nilotinib
Origin:
EU

Nilotinib Teva Uk (Nilotinib)

Nilotinib, the active ingredient in Nilotinib Teva Uk, is a tyrosine kinase inhibitor presented as a tablet for oral use. It treats chronic myeloid leukemia in its chronic, accelerated and blast phases, targeting malignant cells that express the BCR‑ABL fusion protein.

GNH India supplies Nilotinib Teva Uk as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide. The company adheres to stringent quality standards and provides reliable global distribution.

Manufacturer / TM Owner

Teva Uk Limited

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Indications & Clinical Uses

Nilotinib is indicated for the treatment of chronic myeloid leukemia, a BCR‑ABL driven hematologic malignancy.

  • Chronic myeloid leukemia (chronic phase): reduces leukemic cell proliferation and improves hematologic and cytogenetic response.
  • Chronic myeloid leukemia (accelerated phase): helps achieve molecular remission and disease control.
  • Chronic myeloid leukemia (blast crisis): provides therapeutic benefit when other options are limited.

How It Works

  • Nilotinib selectively inhibits the BCR‑ABL tyrosine kinase, as well as the related c‑KIT and PDGFR kinases. By blocking these enzymes, it disrupts downstream signaling pathways that drive proliferation and survival of malignant leukemic cells, leading to reduced tumor growth and increased apoptosis.

Side Effects

Nilotinib may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Nausea
  • Diarrhea
  • Fatigue
  • Rash
  • Headache
  • Arthralgia

Serious or Rare Side Effects

  • QT interval prolongation
  • Pancreatitis
  • Elevated liver enzymes (hepatotoxicity)
  • Severe neutropenia or thrombocytopenia
  • Severe skin reactions (e.g., Stevens‑Johnson syndrome)
  • Cardiac arrhythmias

Precautions & Warnings

When prescribing Nilotinib, clinicians should observe several safety measures to minimize risk.

  • Monitor cardiac function: perform baseline ECG and periodic checks for QT prolongation.
  • Monitor blood counts: conduct regular complete blood count assessments for neutropenia or thrombocytopenia.
  • Monitor liver enzymes: evaluate hepatic function before and during therapy.
  • Avoid strong CYP3A4 inhibitors: concomitant use may increase nilotinib exposure and toxicity.
  • Store at below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Nilotinib interacts with several medicines that can alter its plasma concentration or cardiac safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may raise nilotinib levels and increase toxicity.
  • QT‑prolonging agents (e.g., quinidine, amiodarone): additive risk of cardiac arrhythmias.
  • Antacids containing aluminum or magnesium: can reduce nilotinib absorption if taken simultaneously.

Moderate Interactions (Monitor Closely)

  • Moderate CYP3A4 inhibitors (e.g., erythromycin, fluconazole): may modestly increase exposure.
  • CYP3A4 inducers (e.g., rifampin, carbamazepine): may lower nilotinib concentrations and reduce efficacy.
  • Warfarin: may require INR monitoring due to potential interaction.

Frequently Asked Questions

Nilotinib Teva Uk is prescribed for chronic myeloid leukemia (CML). It is effective in the chronic, accelerated, and blast phases of CML, targeting the BCR‑ABL fusion protein that drives malignant cell growth. The drug helps achieve hematologic, cytogenetic, and molecular responses in patients with this disease.

Nilotinib works by selectively inhibiting the BCR‑ABL tyrosine kinase, as well as c‑KIT and PDGFR kinases. This inhibition blocks key signaling pathways that promote proliferation and survival of leukemic cells, leading to reduced tumor growth and increased programmed cell death.

The dose of Nilotinib Teva Uk is individualized by the treating physician. Factors such as disease phase, patient weight, liver and kidney function, and concurrent medications influence the prescribed amount. Patients should follow the specific dosing instructions provided by their healthcare professional.

Safety of Nilotinib during pregnancy and lactation has not been established. It is generally contraindicated and should be avoided unless the potential benefit outweighs the risk. Women of child‑bearing potential are advised to use effective contraception throughout treatment and for a period after discontinuation.

To order, submit an enquiry on the product page at gnhindia.com, specifying 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, and any required import documentation.

The primary alternative is imatinib, another BCR‑ABL inhibitor. Nilotinib is more potent and binds with higher affinity, making it effective in some imatinib‑resistant cases. However, it carries a distinct safety profile, including a higher risk of QT prolongation, which requires careful cardiac monitoring.

Store the tablets at or below 25 °C in the original container, protected from moisture and direct light. Keep the product out of reach of children and do not use if the packaging appears damaged. No refrigeration is required for this oral tablet formulation.

Nilotinib Teva Uk is taken orally, usually with a low‑fat meal. Swallow the tablet whole with water; do not crush, chew, or split it unless instructed by a healthcare professional. Patients should follow the dosing schedule prescribed by their clinician and avoid missing doses.

Serious adverse events include QT interval prolongation, severe liver toxicity, pancreatitis, and profound cytopenias such as neutropenia or thrombocytopenia. Patients should seek immediate medical attention if they experience palpitations, jaundice, severe abdominal pain, unusual bleeding, or any signs of cardiac arrhythmia.

Nilotinib should not be used by individuals with known hypersensitivity to nilotinib or any tablet excipients, those with uncontrolled cardiac arrhythmias, significant QT prolongation, or severe hepatic impairment. It is also contraindicated in patients taking prohibited concomitant medicines that strongly affect its metabolism.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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