< Instructions for use: Orally, swallow with a glass of warm water. Treatment duration: Treatment should be continued until the patient fails to benefit clinically or develops intolerable toxicity. Dose adjustment and special instructions for use: Treatment of suspected adverse reactions includes suspending or reducing the dosage of Nexavar (sorafenib). If necessary, reduce the dosage of Nexavar (sorafenib) to once daily or once every other day. Second-rate.(&.).
< Adjust the dose accordingly according to skin toxicity:
< Grade skin adverse reactions: paralysis, hypoesthesia, paresthesia, numbness, painless swelling, erythema or discomfort on hands and feet but does not affect daily activities, etc. If symptoms occur at any time, it is recommended that the dose be adjusted to continue using this product and local treatment be given to eliminate symptoms.
< [Packaging] Tablets/box, aluminum-aluminum packaging.
< [Validity period] Two and a half years.
< [Execution standards] Imported drug registration standards
< [Approval number] Registration certificate number
< [Manufacturer] Indian company