美国食品及药物管理局(FDA)周二建议,“暂停”使用强生(Johnson & Johnson)新冠疫苗。
FDA表示,在施打逾680万剂强生新冠疫苗后,有6人出现罕见及严重血栓。
FDA指出,该局将联同美国疾病控制及预防中心(CDC)审视相关数据,但重申不良事件似乎非常罕见。
FDA说,CDC周三将召开免疫实践咨询委员会会议,以进一步审查上述个案及评估其潜在重要意义,而该局也将独立调查个案。
FDA表示,直至有关过程完成,因此,建议暂停使用该款疫苗。
根据了解,所有6宗血栓个案均涉及女性,患者年龄介于18岁至48岁,而症状在接种后的6天至14天内出现。
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