Recorded Chinese product: 三磷酸腺苷二钠-氯化镁注射液三磷酸腺苷二钠-氯化镁注射液

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

分别熔封的灭菌水溶液是一种在国家药监局注册认定的药品。该药品含有分别熔封的灭菌水溶液-9bf7897e等成分。

该药品关联的活性成分包括:分别熔封的灭菌水溶液Fenbie Rongfeng Demie Junshui Rongye。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:长春精优药业股份有限公司Chinese legal name: 长春精优药业股份有限公司。

您可以探索含有相同成分的其他药品:分别熔封的灭菌水溶液-9bf7897e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: 三磷酸腺苷二钠-氯化镁注射液) is a medicine registered with the national drug regulatory authority. It contains recorded ingredients as active ingredient(s).

Active ingredients associated with this product: 分别熔封的灭菌水溶液Fenbie Rongfeng Demie Junshui Rongye.

Manufacturers recorded for this product: 长春精优药业股份有限公司Chinese legal name: 长春精优药业股份有限公司.

Explore other medicines containing the same ingredient: 分别熔封的灭菌水溶液 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: 三磷酸腺苷二钠-氯化镁注射液Recorded Chinese product: 三磷酸腺苷二钠-氯化镁注射液
  • 剂型Dosage form: 注射剂Injection
  • 规格Specification: A液:每2ml:0.1g,M液:每2ml:32mgRecorded Chinese specification: A液:每2ml:0.1g,M液:每2ml:32mg

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

  • 长春精优药业股份有限公司Chinese legal name: 长春精优药业股份有限公司

注册信息NMPA approval number

  • 批准文号NMPA approval number: 国药准字H22025693

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H22025693

Manufacturer

Chinese legal name: 长春精优药业股份有限公司

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H22025693

生产企业

长春精优药业股份有限公司

适应症

颅脑外伤后综合症及其后遗症的辅助治疗 。

用法用量

静脉滴注。先将本品A液注入5%葡萄糖注射液250~500ml中,混匀,再加入等体积本品M液,混匀。初始滴速控制在每分钟20滴以内,如无异常5分钟后,控制在每分钟50滴以内。1日1次,一次用量5?/?。一次A液1~2支,加M液1~2支,一日1次。或遵医嘱。

不良反应

静脉滴速过快有降压作用,可引起胸闷、全身灼热感,停药或减慢滴速可恢复正常水平。

禁忌

1.对本品过敏者禁用。|2.新患心肌梗死与脑出血患者禁用。

注意事项

1.对于用药过程中出现胸闷的患者,如调整滴速后仍有胸闷感,禁止滴注。|2.当药品性状发生改变时禁止使用。|3.对本品过敏者禁用。|4.新患心肌梗死与脑出血患者禁用。

贮藏

密封,在阴凉处干燥处保存。

规格

A液:每2ml:0.1g,M液:每2ml:32mg

证据Evidence

  • 批准文号: 国药准字H22025693
  • 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.