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- 详情
- 别名
- pethidine meperidine
- 分类
- 阿片类 习惯形成 抑制剂
- 后遗时间
- 2-10 小时
- 剂量
- 口服
- 常规
- 100-200mg
- 轻度
- 50-100mg
- 强效
- 200-400mg+
- 持续时间
- 4-6 小时
- 效应
- Euphoria Dry Mouth Mood lift Itchiness Relaxant Constipation Pupil constriction Analgesia
- 起效时间
- 30-60 分钟
- 名称
- demerol
- 通用名
- Pethidine
- 属性
- 后遗效应
- 2–10 小时.
- 别名
- pethidine meperidine
- avoid
- All other CNS depressants.
- 生物利用度
- Oral 50-60% | Rectal 55% | Intramuscular 80-85%
- 分类
- 阿片类 习惯形成 抑制剂
- 剂量
- Light: 50-100mg Common: 100-200mg Strong: 200-400mg+
- 持续
- 4–6 小时.
- 效应
- Euphoria, Dry Mouth, Mood lift, Itchiness, Relaxant, Constipation, Pupil constriction, Analgesia.
- 起效
- 30–60 分钟
- 摘要
A phenylpiperidine opioid first synthesised by Otto Eisleb in 1939, better known by the names meperidine and pethidine. An analgesic once widely prescribed, it has since declined in usage due to the discovery of a toxic metabolite - norpethidine. The drug additionally reacts dangerously with many drugs.
来源与许可
TripSit · 药物资料
TripSit 数据规则：仅限非商业使用，需署名并在每个展示页附来源链接；组合数据仅为快速参考，需结合个体研究判断。
Reference snapshot, not a forum post. Source: TripSit. Noncommercial reuse with TripSit attribution and a source link on every display page; combination data is a quick reference requiring further individual research. https://wiki.tripsit.me/wiki/Factsheets ; https://wiki.tripsit.me/wiki/Drug_combinations . The package.json ISC software tag does not replace these data-specific terms.
Raw source: https://raw.githubusercontent.com/TripSit/drugs/83670cb6bc8863615fcb9be081c87f061b42dea4/drugs.json
Fetched at: 2026-10-23T07:01:06.728397+00:00
Record key: drug:demerol
来源主页：https://wiki.tripsit.me/wiki/Factsheets
组合说明：https://wiki.tripsit.me/wiki/Drug_combinations