美国食品及药物管理局(FDA)周四批准瑞德西韦(Remdesivir)成为首款可用于治疗新冠肺炎的药物。
该种通过静脉注射的抗病毒药物是美国总统特朗普确诊新冠肺炎时所使用的药物之一。
瑞德西韦由总部设在加州的吉利德(Gilead)药厂研发,以Veklury作为商品名销售,是给住院患者作静脉注射的药物。瑞德西韦在春季开始已在美国获紧急使用授权。
瑞德西韦可用于12岁或以上、体重40公斤或以上的住院新冠肺炎病人,至于12岁以下的病人,美国食品及药物管理局仍容许在某些情况下紧急使用。
无论如何,世界卫生组织(WHO)上周曾表示,其全球新冠肺炎疗法试验发现,瑞德西韦对患者的住院时间或存活率并没有显著效果。
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