PMDA drug package insert
ケイキサレート散
PMDA Prescription drug · 鳥居薬品株式会社 · package insert Dec 12, 2023
Key facts
| Brand names | ケイキサレート散 |
|---|---|
| Nonproprietary names | ポリスチレンスルホン酸ナトリウム |
| Companies | 製造販売元／鳥居薬品株式会社, 提携先／sanofi |
| Product type | Prescription drug |
| Therapeutic category | 高カリウム血症改善剤 |
| Therapeutic category codes | 87219 |
| YJ codes | 2190009A1048 |
| Approval numbers | 21900AMX00073000 |
| Package insert edition | 第2版 |
| Package insert date | Dec 12, 2023 |
| PMDA document key | 480306_2190009A1048_1 |
| PMDA company code | 480306 |
At a glance
- 1–9 Package insert revisions
- 1–9 Related PMDA documents
- None Safety communications
- No 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: