Xieyi Li (协一力)协一力

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

利鲁唑是一种在国家药监局注册认定的药品。该药品含有利鲁唑-48aece48等成分。

该药品关联的活性成分包括:利鲁唑Lilu Zuo。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:鲁南贝特制药有限公司Chinese legal name: 鲁南贝特制药有限公司。

您可以探索含有相同成分的其他药品:利鲁唑-48aece48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: 协一力) is a medicine registered with the national drug regulatory authority. It contains recorded ingredients as active ingredient(s).

Active ingredients associated with this product: 利鲁唑Lilu Zuo.

Manufacturers recorded for this product: 鲁南贝特制药有限公司Chinese legal name: 鲁南贝特制药有限公司.

Explore other medicines containing the same ingredient: 利鲁唑 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: 协一力Recorded Chinese name: 协一力
  • 剂型Dosage form: 胶囊剂Capsules
  • 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

  • 鲁南贝特制药有限公司Chinese legal name: 鲁南贝特制药有限公司

注册信息NMPA approval number

  • 批准文号NMPA approval number: 国药准字H20051886

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H20051886

Manufacturer

Chinese legal name: 鲁南贝特制药有限公司 (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

Keep tightly closed.

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H20051886

生产企业

鲁南贝特制药有限公司(国产)

适应症

1.本品适用于肌萎缩性侧索硬化症的治疗,延长生命或机械换气时间。|2.但不适用于其他形式的运动神经元疾病。

用法用量

1.口服,一次1粒(50mg),一日2次。增加每日给药剂量不会增加药效,但增加不良反应。|2.如漏服一次,按原计划服用下1粒。应在餐前1小时或餐后2小时服药,以降低食物对利鲁唑生物利用度的影响。

不良反应

1.本品常见的不良反应为疲劳、胃部不适及血浆转氨酶水平升高。其他不良反应较少见:胃疼、头疼、呕吐、心跳增加、头晕、嗜睡、过敏反应或胰腺炎症(胰腺炎)。|2.偶见嗜中性粒白细胞减少症。|3.本品可能产生未在此列出的其它不良反应。如在您服用本品时健康状况发生任何变化,请告知您的医师或药师。

禁忌

1.对本品及其主要成份过敏者。|2.肝功不正常或转氨酶水平异常增高者。|3.处于妊娠及哺乳期患者。

注意事项

1.肝脏疾病患者慎用,应定期检查肝功能。如曾有肝脏疾患请告知医师,因为本品可能不适合您。|2.服用本药时应禁止过度饮酒。可能发生白细胞(具有重要的抗感染作用)计数减少。|3.如果有任何发热现象(体温升高),须立即与医生联系。如有任何肾脏疾患,请告知医师。|4.服用本品后如感到眩晕或头晕,不应驾驶或操作机器。

贮藏

密封保存。

规格

50mg

证据Evidence

  • 批准文号: 国药准字H20051886
  • 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.