Vaccine Adverse Event Reporting System 2018

The Vaccine Adverse Event Reporting System (VAERS) 2018 was created by the Food and Drug Administration (FDA) and Centers for Disease Control and Prevention (CDC) to receive reports about adverse events that may be associated with vaccines. No prescription drug or biological product, such as a vaccine, is completely free from side effects.

2018年疫苗不良事件报告系统（VAERS）由食品药品监督管理局（FDA）及疾病控制与预防中心（CDC）联合创建，旨在接收与疫苗接种可能相关的副作用报告。任何处方药物或生物制品，如疫苗，均无法完全免于副作用之影响。