PMDA drug package insert
サビーン点滴静注用500mg
PMDA Prescription drug · キッセイ薬品工業株式会社 · package insert May 7, 2026
Key facts
| Brand names | サビーン点滴静注用500mg |
|---|---|
| Nonproprietary names | デクスラゾキサン |
| Companies | 製造販売元／キッセイ薬品工業株式会社 |
| Product type | Prescription drug |
| Therapeutic category | アントラサイクリン系抗悪性腫瘍剤の血管外漏出治療剤 |
| Therapeutic category codes | 87392 |
| YJ codes | 3929410D1022 |
| Approval numbers | 22600AMX00006000 |
| Package insert edition | 第4版 |
| Package insert date | May 7, 2026 |
| PMDA document key | 230034_3929410D1022_1 |
| PMDA company code | 230034 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- None Safety communications
- Yes PMDA review report published
- No Risk management plan (RMP)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMDA approved drugs and package inserts (Japan)
Japan's PMDA publishes the package insert (添付文書) of every prescription drug, OTC drug and regenerative medical product, with brand and nonproprietary names, YJ codes and approval numbers. Names appear in Japanese as published.
Source: Pharmaceuticals and Medical Devices Agency (PMDA), Japan, package insert database · Source date: