Recorded Chinese product: 塞克硝唑片塞克硝唑片

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

塞克硝唑是一种在国家药监局注册认定的药品。该药品含有塞克硝唑-936bb58e等成分。

该药品关联的活性成分包括：塞克硝唑Saike Xiaozuo。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：丹东医创药业有限责任公司Chinese legal name: 丹东医创药业有限责任公司。

您可以探索含有相同成分的其他药品：塞克硝唑-936bb58e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: 塞克硝唑片) is a medicine registered with the national drug regulatory authority. It contains recorded ingredients as active ingredient(s).

Active ingredients associated with this product: 塞克硝唑Saike Xiaozuo.

Manufacturers recorded for this product: 丹东医创药业有限责任公司Chinese legal name: 丹东医创药业有限责任公司.

Explore other medicines containing the same ingredient: 塞克硝唑 productsProducts containing this recorded ingredient.

Source: MedicineGraph authoritative database. Relationships derived from registered product information.

Same active ingredient相同活性成分

Manufacturer recorded for this product本页记录的生产企业

这是什么What is this

  • 通用名/品名Recorded product name: 塞克硝唑片Recorded Chinese product: 塞克硝唑片
  • 剂型Dosage form: 片剂Tablets
  • 规格Specification: 0.25g0.25 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

Same active ingredient相同活性成分

生产企业Manufacturer

  • 丹东医创药业有限责任公司Chinese legal name: 丹东医创药业有限责任公司

注册信息NMPA approval number

  • 批准文号NMPA approval number: 国药准字H20090237

关联实体Relationships

Products by this manufacturer该企业已记录的药品

相关问题Questions

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H20090237

Manufacturer

Chinese legal name: 丹东医创药业有限责任公司 (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H20090237

生产企业

丹东医创药业有限责任公司(国产)

适应症

硝基咪唑类抗原虫药物。主要用于治疗下列疾病: 1.由阴道毛滴虫引起的尿道炎和阴道炎。 2.肠阿米巴病。 3.肝阿米巴病。 4.贾第鞭毛虫病。

用法用量

口服,餐前服用。用量： 1.阴道毛滴虫引起的尿道炎和阴道炎：成人,2g(8片),单次服用。配偶应同时服用。 2.肠阿米巴病： (1)有症状的急性阿米巴病，成人,2g(8片),单次服用。儿童为30mg/kg,单次服用。 (2)无症状的急性阿米巴病：成人,2g(8片),一日1次,连服3日。儿童为一次30mg/kg,一日1次,连服3日。 3.肝阿米巴病：成人：一日1.5g(6片),一次或分次口服,连服5日。儿童为30mg/kg,一次或分次口服,连服.日。 4.贾第鞭毛虫病：儿童：30mg/kg,单次服用。

不良反应

1.常见不良反应为口腔金属异味。
2.偶见不良反应有消化道紊乱(如恶心、呕吐、腹泻、腹痛)皮肤过敏反应(如皮疹、荨麻疹、瘙痒)?深色尿、白细胞减少(停药后恢复正常)。
3.罕见不良反应:眩晕、头痛、中度的神经功能紊乱。

禁忌

以下患者禁用
1.对塞克硝唑或一般硝基咪唑类药物过敏者。
2.妊娠期及哺乳期妇女。
3.有血液疾病史的患者禁用。

注意事项

1.血液异常即往史的患者慎服本品。
2.服药期间禁饮酒精类饮料或饮酒。
3.应放在儿童触不到的地方。

贮藏

遮光，密封保存

规格

0.25g

证据Evidence

  • 批准文号: 国药准字H20090237
  • 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.