


Another NameNexavar、多吉美、索拉非尼
Indications
Indicated for the treatment of unresectable hepatocellular carcinoma, advanced renal cell carcinoma, and progressive differentiated thyroid cancer that is refractory to radioactive iodine therapy.
Specs

Factory:Lucius Pharmaceuticals
Reg No.:10 L 1224/24
Inspection No.:2562-24
Dosage form:Tablet
Indate:24 months
Sorafenib was initially approved in the United States in 2005, and the latest revised prescribing information is dated August 2023.
Indicated for adult patients with unresectable hepatocellular carcinoma, advanced renal cell carcinoma, or radioactive iodine-refractory differentiated thyroid cancer.
The recommended dosage is 400 mg twice daily, taken on an empty stomach.
Patients of reproductive potential should use effective contraception; no dose adjustment is required in elderly patients or those with mild to moderate hepatic or renal impairment.
Overdosage may present with diarrhea and skin reactions; discontinue the drug and provide supportive care.
After oral absorption, sorafenib is metabolized in the liver, with a half-life of approximately 25–48 hours.

Lucius Pharmaceutical Co., Ltd., was established in 2020 in Vientiane, the capital of Laos. It aims to offer safe, effective, and affordable medicines globally. With a factory spanning 25,000 square meters, the company manufactures 200+ generic drugs in diverse therapeutic fields.
Address: No.26 Thongmang village, Xaythany district, Vientiane Capital, Laos
E-mail:laoslucius@gmail.com

Name: Lucius

Telegram name: Vira
No.:0085253923643
Telegram name: Vira
No.:0085253923643