Kewei Jia (可维加)可维加

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

枸橼酸钾是一种在国家药监局注册认定的药品。该药品含有枸橼酸钾-47d8cb1c等成分。

该药品关联的活性成分包括:枸橼酸钾Juyuan Suanjia。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:山东绿叶制药有限公司Chinese legal name: 山东绿叶制药有限公司。

您可以探索含有相同成分的其他药品:枸橼酸钾-47d8cb1c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: 可维加) is a medicine registered with the national drug regulatory authority. It contains recorded ingredients as active ingredient(s).

Active ingredients associated with this product: 枸橼酸钾Juyuan Suanjia.

Manufacturers recorded for this product: 山东绿叶制药有限公司Chinese legal name: 山东绿叶制药有限公司.

Explore other medicines containing the same ingredient: 枸橼酸钾 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: 可维加Recorded Chinese name: 可维加
  • 剂型Dosage form: 颗粒剂Granules
  • 规格Specification: 1.45g1.45 g

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

  • 山东绿叶制药有限公司Chinese legal name: 山东绿叶制药有限公司

注册信息NMPA approval number

  • 批准文号NMPA approval number: 国药准字H10970220

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H10970220

Manufacturer

Chinese legal name: 山东绿叶制药有限公司 (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H10970220

生产企业

山东绿叶制药有限公司(国产)

适应症

用于防治各种原因引起的低钾血症。

用法用量

温开水冲服,每次1-2包,一日三次或遵医嘱。

不良反应

1.口服可有异味感及胃肠道刺激症状,如恶心、呕吐、腹痛、腹泻。在空腹、剂量较大
及原有胃肠道疾病者更易发生。
2.高钾血症。应用过量或原有肾功能损害时易发生,表现为软弱、乏力、手足口唇麻木、不明原因的
焦虑、意识模糊、呼吸困难、心率减慢、心律失常、传导阻滞、甚至心脏骤停。心电图表现为高而尖
的T波、并逐渐出现P-R间期延长、P波消失、QRs波变宽、出现正弦波。

禁忌

伴有少尿或氮质血症的严重肾功能损害患者、未经治疗的阿狄森氏病( Addison s disease )、急性脱水、中暑性痉挛、无尿、严重心肌损害、家族性周期性麻痹和各种原因引起的高血钾患者。

注意事项

1.用药期间注意复查血钾浓度。
2.排尿量低于正常水平的患者慎用。
3.餐后服用以避免本品盐类缓泻作用。
4.服用本品时应当用适量液体冲服,防止摄入高浓度钾盐制剂而产生对胃肠损伤的作用。

贮藏

密封,在阴凉(不超过20℃)干燥处保存。

规格

1.45g

证据Evidence

  • 批准文号: 国药准字H10970220
  • 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.