Wei Ze (维泽)维泽
This is a medicine registration record from NMPA data.本页为国家药监局药品注册记录。
Labeled sections from the recorded Chinese source are included below. English wording is a reference translation when one is on file, not an official English label.本记录未接入产品级适应症/安全性标注字段。
生产企业Manufacturer
- 江苏豪森药业股份有限公司Chinese legal name: 江苏豪森药业股份有限公司
主要成分Active Ingredients
- 枸橼酸钠Juyuan Suanna
- 枸橼酸Juyuan Suan
- 注射用水Water for Injection (注射用水)
- 昂丹司琼ondansetron
药物知识说明
枸橼酸钠是一种在国家药监局注册认定的药品。该药品含有昂丹司琼、枸橼酸、枸橼酸钠-9e05942f等成分。
该药品关联的活性成分包括：昂丹司琼ondansetron、枸橼酸Juyuan Suan、枸橼酸钠Juyuan Suanna、注射用水。这些成分信息来自国家药监局数据库。
该药品标注的生产企业为：江苏豪森药业股份有限公司Chinese legal name: 江苏豪森药业股份有限公司。
您可以探索含有相同成分的其他药品：昂丹司琼-6ddb88c1成分药品。
本页面内容来自国家药监局数据库，MedicineGraph在此基础上提供关系图谱和知识导航。
Medicine Knowledge
This medicine (original name: 维泽) is a medicine registered with the national drug regulatory authority. It contains ondansetron and other recorded ingredients as active ingredient(s).
Active ingredients associated with this product: 昂丹司琼ondansetron, 枸橼酸Juyuan Suan, 枸橼酸钠Juyuan Suanna.
Manufacturers recorded for this product: 江苏豪森药业股份有限公司Chinese legal name: 江苏豪森药业股份有限公司.
Explore other medicines containing the same ingredient: 昂丹司琼 productsondansetron products.
Source: MedicineGraph authoritative database. Relationships derived from registered product information.
这是什么What is this
- 通用名/品名Recorded product name: 维泽Recorded Chinese name: 维泽
- 剂型Dosage form: 注射剂Injection
- 规格Specification: 100ml:昂丹司琼8mg与氯化钠0.9g。Recorded Chinese description: 100ml:昂丹司琼8mg与氯化钠0.9g。
本段仅展示注册/说明书已记录的身份属性，不含适应症或用法建议。Identity attributes from registration/leaflet records only; no indications or usage advice.
主要成分Ingredients
生产企业Manufacturer
- 江苏豪森药业股份有限公司Chinese legal name: 江苏豪森药业股份有限公司
注册信息NMPA approval number
- 批准文号NMPA approval number: 国药准字H20040650
关联实体Relationships
相关问题Questions
信息来源Source and scope
国家药品监督管理局（中国）药品注册数据及已接入说明书字段。National Medical Products Administration (China) medicine-registration data and linked leaflet fields.
- 品名来源Name source: 10多万条药品说明书数据库 (HIGH)Package-insert database (more than 100,000 records) (HIGH)
- 生产企业来源Manufacturer source: 10多万条药品说明书数据库Package-insert database (more than 100,000 records)
- 剂型来源Dosage-form source: 10多万条药品说明书数据库Package-insert database (more than 100,000 records)
范围：当前 MedicineGraph 注册记录及已记录的精确关系；非完整目录，亦不构成疗效等同主张，也不支持换用判断。不含适应症/安全性推断。Scope: current MedicineGraph registration records and exact recorded relationships; not a complete catalog and not a claim of therapeutic equivalence. No inferred indications/safety.
本段为已核准说明书原文摘录（非改写、非AI摘要），非正式英文标签，亦不构成用药建议。 Not an official English label and not medical advice. English wording, when shown, is a reference translation of the Chinese source label.
English translation for reference. Translated from the Chinese source label. Not an official English label and not medical advice.
NMPA approval number
国药准字H20040650
Manufacturer
Chinese legal name: 江苏豪森药业股份有限公司 (domestically manufactured)
Indications
English translation unavailable. The original Chinese source label remains available below.
Dosage and administration
English translation unavailable. The original Chinese source label remains available below.
Adverse reactions
English translation unavailable. The original Chinese source label remains available below.
Contraindications
English translation unavailable. The original Chinese source label remains available below.
Precautions
English translation unavailable. The original Chinese source label remains available below.
Storage
English translation unavailable. The original Chinese source label remains available below.
Specification
English translation unavailable. The original Chinese source label remains available below.
中文说明书原文Original Chinese source label
批准文号
国药准字H20040650
生产企业
江苏豪森药业股份有限公司(国产)
适应症
盐酸昂丹司琼氯化钠注射液用于由白细胞毒性药物化疗和放射治疗引起的恶心呕吐，也适用于预防和治疗手术后的恶心呕吐。
用法用量
本品供静脉滴注用药。给药剂量和途径视呕吐严重程度而定。成人剂量一般每天8mg(1瓶)。对于高度催吐的化疗药引起的呕吐，在化疗前30分钟，化疗后4小时，8小时各静脉滴注本品8mg(1瓶)，停止化疗以后每8~12小时口服片剂8mg；对于催吐程度不太强的化疗药引起的呕吐，化疗前30分钟静脉滴注本品8mg(1瓶)，以后每8~12小时口服片剂8mg，连续5天；对放射治疗引起的呕吐，首剂应于放疗前1~2小时口服片剂8mg，以后每8小时口服8mg。用于预防或治疗手术后呕吐，成人可于麻醉诱导同时静脉滴注本品4mg，对于已出现术后呕吐，可缓慢静脉滴注本品4mg进行治疗。输注时间应不小于15分钟。
不良反应
可有头痛，头部和上腹部有温热感，腹部不适，便秘，口干，皮疹，注射部位局部反应，偶见支气管哮喘或过敏反应，暂时性无症状氨基转移酶升高，上述反应一般轻微，不需特殊处理。偶见运动失调、癫痫发作，胸痛、心律不齐、低血压、心动过缓等罕见报道。
禁忌
对本品有过敏反应者禁用。胃肠道梗阻者禁用。
注意事项
本说明中所涉及到的使用剂量均以昂丹司琼计。|肾衰竭病人无需调整剂量、用药次数和给药途径。肝脏功能中度或严重衰竭病人，本品在体内消除能力显著下降，血清半衰期也显著延长，因此用药剂量每天不应超过8mg。在化疗前可静脉滴注地塞米松磷酸钠，以缓解病人的不适症。不宜用于心功能不全病人。
贮藏
遮光、室温（10~30℃）密闭保存。
规格
100ml:昂丹司琼8mg与氯化钠0.9g。
信息来源Source and scope
国家药品监督管理局（中国）药品注册数据。National Medical Products Administration (China) medicine-registration data.
范围：当前 MedicineGraph 注册记录及已记录的精确关系；非完整目录，亦不构成疗效等同主张，也不支持换用判断。Scope: current MedicineGraph registration records and exact recorded relationships; not a complete catalog and not a claim of therapeutic equivalence.