摘要
andexanet alfa是凝血因子Ⅹa直接抑制剂的特异性逆转剂,于2018年5月3日由美国食品和药物管理局批准上市,用于逆转利伐沙班、阿哌沙班的抗凝作用。andexanet alfa需弹丸式静脉注射,随后给予2 h持续静脉输注的给药方案,具有良好的安全性。
Andexanet alfa has been developed as reversal agent for factor Ⅹ a direct inhibitors, which has been approved to reverse anticoagulation of rivaroxaban and apixaban by the U.S. Food and Drug Administration on May 3, 2018. Andexanet alfa should be administered as an intravenous(IV) bolus, followed by continuous infusion for up to 2 hours, which has demonstrated a good safety.
作者
赵淑娟
洪雪姣
马培志
赵飞
陈博雅
曹晶晶
ZHAO Shu-juan;HONG Xue-jiao;MA Pei-zhi;ZHAO Fei;CHEN Bo-ya;CAO Jing-jing(Department of Pharmacy,People's Hospital of He-nan Province,Zhengzhou HE-NAN 450003,China)
出处
《中国新药与临床杂志》
CAS
CSCD
北大核心
2019年第1期14-18,共5页
Chinese Journal of New Drugs and Clinical Remedies
基金
河南省医学科技攻关计划项目(201702235)