Saifu Mei (赛福美)赛福美
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
- 云南昊邦制药有限公司Chinese legal name: 云南昊邦制药有限公司
主要成分Active Ingredients
- 草乌甲素Caowu Jiasu
- 三醇--乙基
药物知识说明
草乌甲素是一种在国家药监局注册认定的药品。该药品含有草乌甲素-c0b3ec65等成分。
该药品关联的活性成分包括：草乌甲素Caowu Jiasu。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：云南昊邦制药有限公司Chinese legal name: 云南昊邦制药有限公司。
您可以探索含有相同成分的其他药品：草乌甲素-c0b3ec65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: 赛福美) is a medicine registered with the national drug regulatory authority. It contains recorded ingredients as active ingredient(s).
Active ingredients associated with this product: 草乌甲素Caowu Jiasu.
Manufacturers recorded for this product: 云南昊邦制药有限公司Chinese legal name: 云南昊邦制药有限公司.
Explore other medicines containing the same ingredient: 草乌甲素 productsProducts containing this recorded ingredient.
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: 赛福美Recorded Chinese name: 赛福美
- 剂型Dosage form: 片剂Tablets
- 规格Specification: 0.4mg*12片0.4 mg × 12 tablets
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
- 云南昊邦制药有限公司Chinese legal name: 云南昊邦制药有限公司
注册信息NMPA approval number
- 批准文号NMPA approval number: 国药准字H20057421
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H20057421
Manufacturer
Chinese legal name: 云南昊邦制药有限公司 (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
0.4 mg × 12 tablets
中文说明书原文Original Chinese source label
批准文号
国药准字H20057421
生产企业
云南昊邦制药有限公司(国产)
适应症
用于风湿性及类风湿性关节炎、腰肌劳损、肩周炎、四肢扭伤、挫伤等。
用法用量
口服。一次1片，一日2-3次。
不良反应
极少数病人用药后可出现短暂性轻度心慌、恶心、唇舌发麻及心悸等。
禁忌
1．心脏病患者禁用。
2．孕妇及哺乳期妇女禁用。
3．对本品过敏者禁用。
注意事项
1．两次用药相隔时间不宜少于6小时。
2．出现不良反应时，可静脉注射高渗葡萄糖加维生素C，也可注射阿托品，并应减量或停用；反应极重者，可按乌头中毒处理，并停药。
3．当药品性状发生改变时禁止使用。
贮藏
避光，阴凉干燥处（不超过20℃）保存。
规格
0.4mg*12片
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.