[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"$fdYsriHghvl_OcQatcj4lhK9TFC6RFJs4tzJEYPbQtjI":3},{"id":4,"source":5,"question":6,"options":7,"answer":12,"related":13,"type":24,"origin":112,"createTime":26},1073924665,"v2","某药品生产企业生产的药品,造成患者人身损害,经当地的消费者协会调解,企业赔偿患者部分合理费用.该药品生产企业的损害赔偿属于( )",[8,9,10,11],"民事责任","行政处罚","行政处分","刑事责任",[],[14,27,37,41,51,61,71,82,92,102],{"id":15,"source":5,"question":16,"options":17,"answer":22,"related":23,"type":24,"origin":25,"createTime":26},1073924641,"根据药品管理法律法规及相关文件的规定,应当在指定的药品零售企业销售,一般每张处方不得超过7日常用量的是( )",[18,19,20,21],"血液制品","第二类精神药品","含麻黄碱类复方制剂","第一类精神药品",[],[],0,null,"2025-12-26T08:15:39+08:00",{"id":28,"source":5,"question":29,"options":30,"answer":35,"related":36,"type":24,"origin":25,"createTime":26},1073924645,"中华人民共和国境内药品经营许可的说法,错误的是( )",[31,32,33,34],"药品上市许可持有人自行批发药品的,需办理《药品经营许可证》","开办药品批发企业(含药品零售连锁企业总部)的,应当向省级药品监督管理部门申请,经审批同意,依法获取《药品经营许可证》后,方可开展相应药品经营活动","开办药品零售企业(含药品零售连锁企业门店)的,应当向县级以上药品监督管理部门申请,经审批同意,依法获取《药品经营许可证》后,方可开展相应药品经营活动","药品上市许可持有人自行零售药品的,需办理《药品经营许可证》",[],[],{"id":4,"source":5,"question":6,"options":38,"answer":39,"related":40,"type":24,"origin":25,"createTime":26},[8,9,10,11],[],[],{"id":42,"source":5,"question":43,"options":44,"answer":49,"related":50,"type":24,"origin":25,"createTime":26},1073924693,"根据处方药与非处方药分类管理的相关规定,关于非处方药遴选原则解释的说法,错误的是( )",[45,46,47,48],"应用安全,系指经过长明临床使用证实,药品无潜在毒性,不易引起蓄积中毒,基本无不良反应,不引起依赖性","疗效确切,系指药物针对性强,功能主治明确,不需要调整剂量,连续使用不易引起耐药性","质量稳定,系指药品质量可控、性质稳定","使用方便,系指不用经过特殊检查和试验即可使用,以口服和外用的常用剂型为主",[],[],{"id":52,"source":5,"question":53,"options":54,"answer":59,"related":60,"type":24,"origin":25,"createTime":26},1073924715,"关于药品包装、标签和说明书的说法,错误的是( )",[55,56,57,58],"处方药、非处方药、外用药、特殊管理的药品等专用标识在说明书首页的右上方标注","药品包装应当适合药品质量的要求,方便储存、运输和医疗使用,药品的包装分为内包装和外包装","药品批准文号是鉴别假药的重要依据之一","药品有效期是鉴别劣药的重要依据之",[],[],{"id":62,"source":5,"question":63,"options":64,"answer":69,"related":70,"type":24,"origin":25,"createTime":26},1073924740,"根据《野生药材资源保护管理条例》,资源严重减少的主要常用野生药材对应的物种属于( )",[65,66,67,68],"一级保护野生药材物种","中药品种保护物种","二级保护野生药材物种","三级保护野生药材物种",[],[],{"id":72,"source":5,"question":73,"options":74,"answer":79,"related":80,"type":81,"origin":25,"createTime":26},1073924784,"基本药物目录在保持数量相对稳定的基础上,实行动态管理.在此过程中调整品种和数量的因素包括( )",[75,76,77,78],"已上市药品循证医学、药物经济学评价","药品不良反应监测评价","我国疾病谱变化","基本医疗卫生需求和基本医疗保障水平变化",[],[],1,{"id":83,"source":5,"question":84,"options":85,"answer":90,"related":91,"type":24,"origin":25,"createTime":26},1073924793,"根据《中药品种保护条例》,对特定疾病有显著疗效的中药属于( )",[86,87,88,89],"四级保护品种","三级保护品种","一级保护品种","二级保护品种",[],[],{"id":93,"source":5,"question":94,"options":95,"answer":100,"related":101,"type":24,"origin":25,"createTime":26},1073924802,"境外生产的化学药品的批准文号格式是( )",[96,97,98,99],"国药准字S + 4位年号 + 4位顺序号","国药准字Z + 4位年号 + 4位顺序号","J + 4位年号 + 4位顺序号","国药准字HJ + 4位年号+ 4位顺序号",[],[],{"id":103,"source":5,"question":104,"options":105,"answer":110,"related":111,"type":24,"origin":25,"createTime":26},1073924816,"国家药品监督管理部门建立化学原料药、辅料及直接接触药品的包装材料和容器关联审评审批制度.这种制度是( )",[106,107,108,109],"在审批药品制剂时,对化学原料药一并审评审批,对相关辅料、直接接触药品的包装材料和容器一并审评","在审批药品制剂时,对化学原料药、相关辅料、直接接触药品的包装材料和容器一并审评审批","在审批药品制剂时,对化学原料药、相关辅料、直接接触药品的包装材料和容器一并审评","在审批药品制剂时,对相关辅料、直接接触药品的包装材料和容器一并审评审批,对化学原料药一并审评",[],[],{"courseName":113,"courseImg":114,"workName":115,"workId":115,"count":24,"courseId":116},"[共享课]药事管理学","https:\u002F\u002Ftihai-oss-cloud.itihey.com\u002Fimg\u002F21b85d13a2e5052f0333856f7babad3e.jpg","","1000050195"]