PMDA drug package insert
リサイオ点滴静注液100mg
PMDA Prescription drug · 住友ファーマ株式会社 · package insert Apr 1, 2022
Key facts
| Brand names | リサイオ点滴静注液100mg |
|---|---|
| Nonproprietary names | チオテパ |
| Companies | 製造販売元／住友ファーマ株式会社 |
| Product type | Prescription drug |
| Therapeutic category | 造血幹細胞移植前治療薬 |
| Therapeutic category codes | 874212 |
| YJ codes | 4212400A1021 |
| Approval numbers | 23100AMX00292 |
| Package insert edition | 第2版 |
| Package insert date | Apr 1, 2022 |
| PMDA document key | 400093_4212400A1021_1 |
| PMDA company code | 400093 |
At a glance
- 1–9 Package insert revisions
- 10–99 Related PMDA documents
- None Safety communications
- Yes PMDA review report published
- Yes 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: