Purchase Nilotinib (Tasigna) capsules online:

How and where to order Tasigna (Nilotinib) 200 mg capsules online:

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Prices: from $22.07 per pill
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Forms: Nilotinib (Tasigna) 200 mg capsules
Quantity: 28, 56 pills
Type: Tasigna brand and generics
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Indications and usage:

Tasigna (Nilotinib) is a kinase inhibitor indicated for the treatment of:

  • Adult and pediatric patients greater than or equal to 1 year of age with newly diagnosed Philadelphia chromosome positive chronic myeloid leukemia (Ph+ CML) in chronic phase.
  • Adult patients with chronic phase (CP) and accelerated phase (AP) Ph+ CML resistant to or intolerant to prior therapy that included imatinib.
  • Pediatric patients greater than or equal to 1 year of agewith Ph+ CML-CP resistant or intolerant to prior tyrosine-kinase inhibitor (TKI) therapy.


    Dosage and administration:

  • Recommended adult dose: newly diagnosed Ph+ CML-CP: 300 mg orally twice daily. Resistant or intolerant Ph+ CML-CP and CML-AP: 400 mg orally twice daily.
  • Recommended pediatric dose: newly diagnosed Ph+ CML-CP or Ph+ CML-CP resistant or intolerant to prior TKI therapy: 230 mg/m2orally twice daily, rounded to the nearest 50 mg dose (to a maximum single dose of 400 mg).
  • See dosage and administration for full dosing instructions and dose-reduction instructions for toxicity.
  • Reduce starting dose in patients with baseline hepatic impairment.
  • Eligible newly diagnosed adult patients with Ph+ CML-CP who have received this medication for a minimum of 3 years and have achieved a sustained molecular response (MR4.5) and patients with Ph+ CML-CP resistant or intolerant to imatinib who have received Tasigna for at least 3 years and have achieved a sustained molecular response (MR4.5) may be considered for treatment discontinuation.


    Dosage forms and strengths:

    Tasigna (Nilotinib) capsules: 50 mg, 150 mg, and 200 mg


    Contraindications:

    Nilotinib is contraindicated in patients with hypokalemia, hypomagnesemia, or long QT syndrome.


    Warnings and precautions:

  • Myelosuppression: monitor complete blood count (CBC) during therapy and manage by treatment interruption or dose-reduction.
  • Cardiac and arterial vascular occlusive events: evaluate cardiovascular status, monitor and manage cardiovascular risk factors during Tasigna therapy.
  • Pancreatitis and elevated serum lipase: monitor serum lipase; if elevations are accompanied by abdominal symptoms, interrupt doses and consider appropriate diagnostics to exclude pancreatitis.
  • Hepatotoxicity: monitor hepatic function tests monthly or as clinically indicated.
  • Electrolyte abnormalities: Tasigna can cause hypophosphatemia, hypokalemia, hyperkalemia, hypocalcemia, and hyponatremia. Correct electrolyte abnormalities prior to initiating Nilotinib and monitor periodically during therapy.
  • Tumor lysis syndrome: maintain adequate hydration and correct uric acid levels prior to initiating therapy with this medicine.
  • Hemorrhage: hemorrhage from any site may occur. Advise patients to report signs and symptoms of bleeding and medically manage as needed.
  • Fluid retention: monitor patients for unexpected rapid weight gain, swelling, and shortness of breath. Manage medically.
  • Effects on growth and development in pediatric patients: growth retardation has been reported in pediatric patients treated with Tasigna. Monitor growth and development in pediatric patients.
  • Embryo-fetal toxicity: advise patients of potential risk to a fetus and to use effective contraception.
  • Treatment discontinuation: patients must have typical BCR-ABL transcripts. An FDA-authorized test with a detection limit below MR4.5 must be used to determine eligibility for discontinuation. Patients must be frequently monitored by the FDA authorized testto detect possible loss of remission.


    Overdosage:

    Overdose with nilotinib has been reported, where an unspecified number of Tasigna capsules were ingested in combination with alcohol and other drugs. Events included neutropenia, vomiting, and drowsiness. In the event of overdose, the patient should be observed and appropriate supportive treatment given.


    Adverse reactions, side effects:

    The most commonly reported non-hematologic adverse reactions of nilotinib pills ( >= 20%) in adult and pediatric patients were nausea, rash, headache, fatigue, pruritus, vomiting, diarrhea, cough, constipation, arthralgia, nasopharyngitis, pyrexia, and night sweats. Hematologic adverse drug reactions include myelosuppression: thrombocytopenia, neutropenia, and anemia. The adverse reactions include growth retardation in 2 adolescent patients and growth hormone deficiency with short stature in the remaining patient.

    To report suspected side effects of Tasigna (Nilotinib) capsules, contact Novartis pharmaceutical company or your local FDA.


    Drug interactions:

  • Strong CYP3A inhibitors: avoid concomitant use with Tasigna, or reduce it dose if co-administration cannot be avoided.
  • Strong CYP3A inducers: avoid concomitant use with this medication.
  • Proton pump inhibitors: use short-acting antacids or H2 blockers as an alternative to proton pump inhibitors.


    Use in specific populations:

  • Sexually active female patients should use effective contraception during treatment.
  • Should not breast-feed.
  • No data to support use in pediatrics.
  • A lower starting dose of nilotinib is recommended in patients with hepatic impairment.