Ke Su (可素)可素

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

主要成分Active Ingredients

药物知识说明

注射用水是一种在国家药监局注册认定的药品。该药品含有注射用水、苦参碱-c2005456等成分。

该药品关联的活性成分包括:注射用水、苦参碱Kushen Jian。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:西安海欣制药有限公司Chinese legal name: 西安海欣制药有限公司。

您可以探索含有相同成分的其他药品:注射用水-4ef6f8fd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: 可素) is a medicine registered with the national drug regulatory authority. It contains recorded ingredients as active ingredient(s).

Active ingredients associated with this product: 苦参碱Kushen Jian.

Manufacturers recorded for this product: 西安海欣制药有限公司Chinese legal name: 西安海欣制药有限公司.

Explore other medicines containing the same ingredient: products 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: 可素Recorded Chinese name: 可素
  • 剂型Dosage form: 注射剂Injection
  • 规格Specification: 50mg50 mg

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

  • 西安海欣制药有限公司Chinese legal name: 西安海欣制药有限公司

注册信息NMPA approval number

  • 批准文号NMPA approval number: 国药准字H20031260

关联实体Relationships

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H20031260

Manufacturer

Chinese legal name: 西安海欣制药有限公司 (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

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H20031260

生产企业

西安海欣制药有限公司(国产)

适应症

用于慢性乙型肝炎的转氨酶升高和胆红索异常。

用法用量

每次0.15g加入10%葡萄糖注射液500ml,缓慢静脉滴注(每分钟不宜超过60滴),每日一次,二个月为一疗程。

不良反应

滴注速度太快会引起头晕或恶心等症状,减慢滴速后即消失。

禁忌

对本品成分过敏者禁用。

注意事项

1、本品只供静脉滴注,滴注速度以每分钟不超过60滴为宜。或在医师指导下使用。

2、避免长期在一个部位注射而造成血管及局部组织损伤。

3、肾功能不全者用量酌减。

贮藏

避光,密闭,阴凉(不超过20℃)干燥处保存。

规格

50mg

证据Evidence

  • 批准文号: 国药准字H20031260
  • rights: 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。

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.