Archived - Notice to Hospitals - Increased mortality and risk of serious adverse events when prophylactic heparin is abruptly discontinued in patients to be started on Xigris [drotrecogin alfa (activated)] for severe sepsis
Archived - Notice to Hospitals - Increased mortality and risk of serious adverse events when prophylactic heparin is abruptly discontinued in patients to be started on Xigris [drotrecogin alfa (activated)] for severe sepsis
Recalling Firm: Marketed health products
Product Description & Identification
Archived - Notice to Hospitals - Increased mortality and risk of serious adverse events when prophylactic heparin is abruptly discontinued in patients to be started on Xigris [drotrecogin alfa (activated)] for severe sepsis
Additional Source Details
| Field | Value |
|---|---|
| N I D | 24210 |
| U R L | https://recalls-rappels.canada.ca/en/alert-recall/archived-notice-hospitals-increased-mortality-and-risk-serious-adverse-events-when |
| Title | Archived - Notice to Hospitals - Increased mortality and risk of serious adverse events when prophylactic heparin is abruptly discontinued in patients to be started on Xigris [drotrecogin alfa (activated)] for severe sepsis |
| Archived | 1 |
| Category | Biologic or vaccine |
| Last updated | 2006-12-22 |
| Organization | Marketed health products |
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Overview
- Recalling FirmMarketed health products
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🚨 SAFETY ALERT: Marketed health products - Archived - Notice to Hospitals - Increased mortality and risk of serious adverse events when prophylactic heparin is abruptly discontinued in patients to be started on Xigris [drotrecogin alfa (activated)] for severe sepsis Check if your household is affected: https://therecallfile.com/recalls/archived-notice-to-hospitals-increased-mortality-and-risk-of-serious-a/CANADA-24210
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