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Regorafenib tablets 40mg/tablet, 28 tablets/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
- Warnings and Precautions
• Bleeding: Serious or life-threatening bleeding should be permanently discontinued from LuciRegor.
• Skin toxicity: interrupt, reduce or discontinue LuciRegor depending on the severity and duration of skin toxicity.
• Blood Pressure: temporarily or permanently discontinue LuciRegor for severe or uncontrollable Blood Pressure.
• Cardiac ischemia and infarction: For new or acute cardiac ischemia/infarction, interrupt LuciRegor and resume only after resolution of the acute ischemic event.
• Reversible posterior leukoencephalopathy syndrome (RPLS): discontinuation of LuciRegor.
• Gastrointestinal perforation or fistula: Discontinue LuciRegor.
• Wound healing complications: Discontinue use of LuciRegor prior to surgery. Patients with open wounds should discontinue use.
• Embryo-fetal toxicity: May cause harm to the fetus. Inform the woman of the potential risks of the fetus. - Medication risks
- Adverse Reactions
The most common adverse effects (≥ 30%) are fatigue/fatigue, decreased appetite and food intake, hand-foot skin response (HFSR) [palmoplantar paresthesia (PPE)], diarrhea, mucositis, weight loss, infection, Blood Pressure, and pronunciation disorders.
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