辉瑞的新冠肺炎口服药Paxlovid周四获得欧洲药品管理局(EMA)的紧急使用授权。
EMA建议各成员国,可开始使用美国药厂辉瑞的抗新冠肺炎口服药Paxlovid,以治疗在染疫初期的成年高风险患者。
不关Paxlovid仍有待全面评估完成,才会正式获得授权。
总部设于荷兰的EMA表示,由于欧盟各地的染疫及死亡数持续上升,因此给予上述紧急建议。患者在确诊或出现症状5天内,但未需要使用呼吸机前应尽早使用该口服药。
据本周公布的数据显示,Paxlovid对预防高风险病人住院及死亡的有效率近90%,而最近的实验室数据则显示该药针对Omicron的效果仍有效。
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