报告药品不良事件/不良反应
如果您使用说明书中注明“北京锐领医药有限公司”或者“Reliaccess”为联系人的进口产品出现了任何副作用,我们鼓励您咨询您的医生、药剂师或护士。锐领医药将收集药品不良事件/不良反应信息,以监控产品安全性,并且调查、评估和向相关生产企业和监管机构报告不良事件/不良反应。
报告药品不良事件/不良反应,请将具体信息和相关资料发送邮件至:Phv.china@reliaccess.cn或致电010-53655935。请注意当您报告药品不良事件/不良反应时,我们会收集您的相关个人信息,这些信息将会内部登记和严格保密。
If you experience any adverse drug events with imported products that indicate "Beijing Reliaccess Medical INC." or "Reliaccess" as the contact person in your user manual, we encourage you to consult your doctor, pharmacist, or nurse. Reliaccess will collect information on adverse drug events/reactions to monitor product safety, then investigate, evaluate, and report adverse events/reactions to relevant production enterprises and regulatory agencies.