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["10969","XL01XEA309E001010101523","2","安罗替尼","","口服常释剂型","限：1.用于既往至少接受过2种系统化疗后出现进展或复发的局部晚期或转移性非小细胞肺癌患者的治疗。对于存在表皮生长因子受体（EGFR）基因突变或间变性淋巴瘤激酶（ALK）阳性的患者，在开始盐酸安罗替尼胶囊治疗前应接受相应的标准靶向药物治疗后进展、且至少接受过2种系统化疗后出现进展或复发。2.用于腺泡状软组织肉瘤、透明细胞肉瘤以及既往至少接受过含蒽环类化疗方案治疗后进展或复发的其他晚期软组织肉瘤患者的治疗。3.用于既往至少接受过2种化疗方案治疗后进展或复发的小细胞肺癌患者的治疗。该适应症是基于一项包括119例既往至少接受过2种化疗方案资料后进展或复发的小细胞肺癌患者的II期临床试验的结果给予的附条件批准。该适应症的完全批准将取决于正在进行的确证性试验证实本品在该人群的临床获益。4.用于具有临床症状或明确疾病进展的、不可切除的局部晚期或转移性甲状腺髓样癌患者的治疗。该适应症是基于一项包括91例晚期甲状腺髓样癌的IIB期临床试验结果给予的附条件批准。该适应症的完全批准将取决于正在进行的确证性试验证实本品在该人群的临床获益。",2017163301,"盐酸安罗替尼胶囊","福可维","硬胶囊剂","10mg","盒","7","铝箔","正大天晴药业集团股份有限公司","1785.00","否","否",163301,"国谈药品"]
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["11172","XL03AAC106B002020203708","2","人粒细胞刺激因子(重组人粒细胞刺激因子)","限白细胞低于2000/μl或粒细胞低于1000/μl或工伤保险。","注射剂","限放化疗后的骨髓抑制",20157199,"人粒细胞刺激因子注射液","里亚金","注射液","0.75ml:0.15mg","支","1","玻璃瓶","哈药集团生物工程有限公司","73.20","否","否",129538]
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["11191","XL03AAC146B001030279189","2","重组人粒细胞刺激因子（CHO细胞）","限白细胞低于2000/μl或粒细胞低于1000/μl或工伤保险。","注射剂","限放化疗后的骨髓抑制",20151336,"注射用重组人粒细胞刺激因子(CHO细胞)","格拉诺赛特","冻干粉针剂","50μg","支","1","空","日本中外制药工业株式会社宇都宫工厂Utsunomiya Plant of Chugai Pharma Manufacturing Co.,Ltd.","153.22","否","否",147343]
["11200","XL03ABC094B014010100510","2","人干扰素α1b(重组人干扰素α-1b)","限用于以下适应证之一，进口产品先由个人自理20%。①各类恶性肿瘤放疗或化疗辅助治疗。每个疗程不超过300万μ×21支，一个结算年度使用不超过2个疗程。②抗肿瘤治疗。用于慢性髓性白血病，毛细胞白血病，多发性骨髓瘤，骨髓增生性疾病，T细胞淋巴瘤，肾癌或恶性黑色素瘤。慢性髓性白血病、毛细胞白血病的治疗期不超过12个月，总剂量不超过300万μ×365支；维持期每月不超过300万μ×12支。多发性骨髓瘤,T细胞淋巴瘤,肾癌,恶性黑色素瘤的治疗期不超过3个月，总剂量600万μ×90支，维持期每月不超过300万μ×12支。③丙型肝炎治疗方案及用法、用量按《丙型肝炎防治指南》执行。④活动性乙型肝炎限传染病专科、副高以上职称，按《乙型肝炎治疗指南》使用，累计使用半年无效时应停药，总疗程不超过12个月，疗程和聚乙二醇干扰素α-2a[α-2b]合并计算。","注射剂","限白血病、淋巴瘤、黑色素瘤、肾癌、多发性骨髓瘤、丙肝、慢性活动性乙肝。丙肝、慢性活动性乙肝连续使用6个月无效时停药，连续使用不超过12个月",2015144761,"注射用人干扰素α1b","赛若金","冻干粉针剂","100万IU(10μg)","支","1","西林瓶","深圳科兴药业有限公司","15.61","否","否",144763]
["11211","XL03ABC095B014020103320","2","人干扰素α2a（重组人干扰素α-2a）","限用于以下适应证之一，进口产品先由个人自理20%。①各类恶性肿瘤放疗或化疗辅助治疗。每个疗程不超过300万μ×21支，一个结算年度使用不超过2个疗程。②抗肿瘤治疗。用于慢性髓性白血病，毛细胞白血病，多发性骨髓瘤，骨髓增生性疾病，T细胞淋巴瘤，肾癌或恶性黑色素瘤。慢性髓性白血病、毛细胞白血病的治疗期不超过12个月，总剂量不超过300万μ×365支；维持期每月不超过300万μ×12支。多发性骨髓瘤,T细胞淋巴瘤,肾癌,恶性黑色素瘤的治疗期不超过3个月，总剂量600万μ×90支，维持期每月不超过300万μ×12支。③丙型肝炎治疗方案及用法、用量按《丙型肝炎防治指南》执行。④活动性乙型肝炎限传染病专科、副高以上职称，按《乙型肝炎治疗指南》使用，累计使用半年无效时应停药，总疗程不超过12个月，疗程和聚乙二醇干扰素α-2a[α-2b]合并计算。","注射剂","限白血病、淋巴瘤、黑色素瘤、肾癌、多发性骨髓瘤、丙肝、慢性活动性乙肝。丙肝、慢性活动性乙肝连续使用6个月无效时停药，连续使用不超过12个月",2015125962,"注射用重组人干扰素α2a","无","冻干粉针剂","500万IU","瓶","1","西林瓶","长春生物制品研究所有限责任公司","38.30","否","否",125961]
["11214","XL03ABC097B002020100070","2","人干扰素α2b(重组人干扰素α-2b)","限用于以下适应证之一，进口产品先由个人自理20%。①各类恶性肿瘤放疗或化疗辅助治疗。每个疗程不超过300万μ×21支，一个结算年度使用不超过2个疗程。②抗肿瘤治疗。用于慢性髓性白血病，毛细胞白血病，多发性骨髓瘤，骨髓增生性疾病，T细胞淋巴瘤，肾癌或恶性黑色素瘤。慢性髓性白血病、毛细胞白血病的治疗期不超过12个月，总剂量不超过300万μ×365支；维持期每月不超过300万μ×12支。多发性骨髓瘤,T细胞淋巴瘤,肾癌,恶性黑色素瘤的治疗期不超过3个月，总剂量600万μ×90支，维持期每月不超过300万μ×12支。③丙型肝炎治疗方案及用法、用量按《丙型肝炎防治指南》执行。④活动性乙型肝炎限传染病专科、副高以上职称，按《乙型肝炎治疗指南》使用，累计使用半年无效时应停药，总疗程不超过12个月，疗程和聚乙二醇干扰素α-2a[α-2b]合并计算。","注射剂","限白血病、淋巴瘤、黑色素瘤、肾癌、多发性骨髓瘤、丙肝、慢性活动性乙肝。丙肝、慢性活动性乙肝连续使用6个月无效时停药，连续使用不超过12个月",2015137750,"人干扰素α2b注射液","凯因益生","注射液","0.5ml:500万IU","盒","1","预充式(预灌封)注射器","北京凯因科技股份有限公司","40.94","否","否",137747]
["11226","XL03ABC098B002030100868","2","人干扰素α2b[重组人干扰素α-2b（假单胞菌）]","限用于以下适应证之一，进口产品先由个人自理20%。①各类恶性肿瘤放疗或化疗辅助治疗。每个疗程不超过300万μ×21支，一个结算年度使用不超过2个疗程。②抗肿瘤治疗。用于慢性髓性白血病，毛细胞白血病，多发性骨髓瘤，骨髓增生性疾病，T细胞淋巴瘤，肾癌或恶性黑色素瘤。慢性髓性白血病、毛细胞白血病的治疗期不超过12个月，总剂量不超过300万μ×365支；维持期每月不超过300万μ×12支。多发性骨髓瘤,T细胞淋巴瘤,肾癌,恶性黑色素瘤的治疗期不超过3个月，总剂量600万μ×90支，维持期每月不超过300万μ×12支。③丙型肝炎治疗方案及用法、用量按《丙型肝炎防治指南》执行。④活动性乙型肝炎限传染病专科、副高以上职称，按《乙型肝炎治疗指南》使用，累计使用半年无效时应停药，总疗程不超过12个月，疗程和聚乙二醇干扰素α-2a[α-2b]合并计算。","注射剂","限白血病、淋巴瘤、黑色素瘤、肾癌、多发性骨髓瘤、丙肝、慢性活动性乙肝。丙肝、慢性活动性乙肝连续使用6个月无效时停药，连续使用不超过12个月",2015140033,"人干扰素α2b注射液","安福隆","注射液","1ml:500万IU","盒","1","预充式(预灌封)注射器","天津未名生物医药有限公司","52.30","否","否",140035]
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["11278","XL03AXK015B002010404726","2","卡介菌多糖、核酸制剂","","注射剂","限慢性支气管炎，慢性过敏性疾病，哮喘。",2015134195,"卡介菌多糖核酸注射液","无","注射液","1ml:含卡介菌多糖0.35mg,核酸不低于40μg","支","1","安瓿","浙江万晟药业有限公司","","否","否",134199,"无联动（采购）价，医保不支付药品"]
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["11362","XL04AAT108B001010100231","2","兔抗人胸腺细胞免疫球蛋白","","注射剂","限器官移植排斥反应高危人群的诱导治疗；急性排斥反应的治疗；重型再生障碍性贫血",2015242208,"兔抗人胸腺细胞免疫球蛋白","即复宁","粉针剂","25mg","支","1","安瓿","法国Genzyme Polyclonals S.A.S.","2360.00","否","否",142208]
["11373","XL04AAT163A001010278724","2","托法替布","","口服常释剂型","限诊断明确的类风湿关节炎经传统DMARDs治疗3-6个月疾病活动度下降低于50%者，并需风湿病专科医师处方。",2018163135,"枸橼酸托法替布片","尚杰","薄膜衣片","5mg(以托法替布计)","瓶","28","塑料瓶","德国Pfizer Manufacturing Deutschland GMBH","785.91","否","否",163135]
["11382","XL04AAY270A001020178679","2","依维莫司","","口服常释剂型","限以下情况方可支付：1.接受舒尼替尼或索拉非尼治疗失败的晚期肾细胞癌成人患者。2.不可切除的、局部晚期或转移性的、分化良好的（中度分化或高度分化）进展期胰腺神经内分泌瘤成人患者。3.无法手术切除的、局部晚期或转移性的、分化良好的、进展期非功能性胃肠道或肺源神经内分泌肿瘤患者。4.不需立即手术治疗的结节性硬化症相关的肾血管平滑肌脂肪瘤（TSC-AML)成人患者。5.不能手术的结节性硬化症相关的室管膜下巨细胞星型细胞瘤的患者。",2016153766,"依维莫司片","飞尼妥","素片","5mg","盒","30","铝塑","瑞士Novartis Pharma Stein AG","3900.00","是","否",153764,"国谈药品"]
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