Vaccine Adverse Event Reporting System 2017

The Vaccine Adverse Event Reporting System (VAERS) 2017 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.

美国食品药品监督管理局（FDA）与疾病控制与预防中心（CDC）共同创建了2017年的疫苗不良事件报告系统（VAERS），旨在接收有关可能与疫苗相关的不良事件的报告。任何处方药物或生物制品，如疫苗，均无法完全免除副作用。