Drug Report History
Below you will find the report version history. When a report is updated, a new version of the report is created. The report history allows you to see the changes between versions. You can select two versions of the report to compare. The fields that were changed between versions will be highlighted in yellow.
The translation of reports creates two separate versions which is why some reports may not seem to have any differences. In this case, only the language field below will be highlighted in yellow.
| Version v2-FR | Version v2-FR | |
|---|---|---|
| Language | French | French |
| Date Updated | 2017-10-31 | 2017-10-31 |
| Drug Identification Number | 02347121 | 02347121 |
| Brand name | NIASTASE RT | NIASTASE RT |
| Common or Proper name | Eptacog Alfa (activated) | Eptacog Alfa (activated) |
| Company Name | NOVO NORDISK CANADA INC | NOVO NORDISK CANADA INC |
| Ingredients | EPTACOG ALFA | EPTACOG ALFA |
| Strength(s) | 2MG | 2MG |
| Dosage form(s) | KIT POWDER FOR SOLUTION | KIT POWDER FOR SOLUTION |
| Route of administration | INTRAVENOUS | INTRAVENOUS |
| Packaging size | One vial of 2mg (100 KIU) per carton | One vial of 2mg (100 KIU) per carton |
| ATC code | B02BD | B02BD |
| ATC description | VITAMIN K AND OTHER HEMOSTATICS | VITAMIN K AND OTHER HEMOSTATICS |
| Reason for discontinuation | Business reasons | Business reasons |
| Anticipated discontinuation date | 2017-10-27 | 2017-10-27 |
| Actual discontinuation date | 2017-10-27 | 2017-10-27 |
| Remaining supply date | 2017-10-27 | 2017-10-27 |
| Discontinuation status | Discontinued | Discontinued |
| Discontinuation decision reversal | no | no |
| Tier 3 Status | No | No |
| Information on remaining supply | ||
| Company comments | ||
| Health Canada comments |