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根据国际医学科学组织委员会(CIOMS)推荐,属于偶见级别的药品不良反应,其发生率范围在()

发布日期:2020-12-11

根据国际医学科学组织委员会(CIOMS)推荐,属于偶见级别的药品不良反应,其发生率范围在()
A

2%~10%

B

1%~2%

C

0.1%~1%

D

0.01%~0.1%

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医学继续教育

执业药师继续教育

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根据国际医学科学组织委员会(CIOMS)推荐,属于偶见级别的药品不良反应,其发生率范围在()

根据国际医学科学组织委员会(CIOMS)推荐,属于偶见级别的药品不良反应,其发生率范围在()

药品不良反应专家咨询委员会由()

药物不良反应的报告范围分为报告药品引起的所有可疑不良反应和药品引起的严重罕见或新的不良反应,其分界年限为(  )。

药物不良反应的报告范围分为报告药品引起的所有可疑不良反应和药品引起的严重罕见或新的不良反应,其分界年限为(  )。

患者用某药后出现不良反应,且与该药物已知的不良反应相符合。停药后不良反应停止,则判定该不良反应发生与所用药物的关系是(  )。

患者用某药后出现不良反应,且与该药物已知的不良反应相符合。停药后不良反应停止,则判定该不良反应发生与所用药物的关系是(  )。

由于药品不良反应()医疗差错或事故,患者()药品不良反应提起医疗诉讼,这就保护医务人员客观、及时地报告药物不良反应。

由于药品不良反应()医疗差错或事故,患者()药品不良反应提起医疗诉讼,这就保护医务人员客观、及时地报告药物不良反应。

2016年全国药品不良反应监测网络累计收到《药品不良反应/事件报告表》达到()