Iclusig (Ponatinib)

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Brand Name : Iclusig

Marketing Authorization Holder : Incyte

Prescription Required

 
 
No Generic Medicine available for this medicine.

Product Details

Iclusig

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According to the European Medicines Agency, brand name Iclusig originating from Europe is manufactured at the following site(s): Incyte Biosciences Distribution B.V. Paasheuvelweg 25 1105 BP Amsterdam NetherlandsTjoapack Netherlands B.V. Nieuwe Donk 9 4879 AC Etten-Leur Netherlands

Information about Iclusig (Ponatinib)

Iclusig (Ponatinib) is a targeted therapy used in the treatment of certain types of leukemia. It is an oral tyrosine kinase inhibitor that specifically targets the BCR-ABL fusion protein, which is commonly associated with chronic myeloid leukemia (CML) and acute lymphoblastic leukemia (ALL).

Product Highlights

  • Designed for patients with specific genetic mutations, including T315I mutation, making it effective for resistant cases.
  • Chronic Myeloid Leukemia (CML) in chronic, accelerated, or blast phases.
  • Acute Lymphoblastic Leukemia (ALL) with the Philadelphia chromosome.
  • Patients with resistance or intolerance to other tyrosine kinase inhibitors.

Key Ingredient

  • Ponatinib

Key Benefits

  • High response rates in patients with resistant mutations.
  • Focused action on BCR-ABL and its mutations.
  • Oral administration simplifies the treatment regimen.

Direction of Use

  • Follow the physician's prescription closely. Initial doses often start at 45 mg once daily, but adjustments may be made based on response and tolerability.
  • Regular blood tests are necessary to monitor for effectiveness and potential side effects.

Safety Concerns

  • Common side effects include hypertension, rash, headache, and myelosuppression (decreased bone marrow function).
  • Risk of arterial occlusive events (heart attack, stroke) and severe liver toxicity.
  • Patients should be monitored for cardiovascular health and liver function during treatment.

Avoid Iclusig (Ponatinib) If

  • Known hypersensitivity to Ponatinib or any of its components.
  • History of serious cardiovascular conditions may contraindicate use.
  • Significant liver dysfunction or disease.
  • Should be avoided because of the potential risks to the fetus or infant.


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