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Crizotinib capsules 250 mg/capsule, 60 capsules/box
Medication Safety Tips
Use this product according to its instructions, medical advice, and your health needs. Shipping is arranged after payment once the order meets dispatch requirements.
- Contraindications
- • Hepatotoxicity: Fatal hepatotoxicity occurred in 0.1% of patients. Regular liver function tests are performed for monitoring. Temporarily discontinue, reduce dose, or permanently discontinue Lucicriz.
• Interstitial lung disease (ILD)/pneumonia: occurs in 2.9% of patients. Permanently discontinue in patients with ILD/pneumonia.
• Prolonged QT interval: 2.1% of patients. Monitor the electrocardiogram and electrolytes of patients with a history of QTc prolongation or who are susceptible to QTc prolongation or who are taking drugs that prolong QT. Temporarily discontinue, reduce dose, or permanently discontinue Lucicriz.
• Bradycardia: Lucicriz can cause bradycardia. Monitor heart rate and blood pressure regularly. Temporarily discontinue, reduce dose, or permanently discontinue Lucicriz.
• Severe vision loss: 0.2% of patients reported this symptom. Lucicriz should be discontinued for patients with severe vision loss. Perform an ophthalmic assessment.
• Embryo-fetal toxicity: May cause harm to the fetus. Women of childbearing potential are advised to be aware of the potential risks to the fetus and to use effective contraception. - Medication risks
- The most common adverse reactions (≥ 25%) are visual impairment, nausea, diarrhea, vomiting, edema, constipation, elevated transaminases, fatigue, decreased appetite, upper respiratory tract infections, dizziness, and neuropathy.
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