FDA Adverse Event
Injury
Summary report: N
SOARIAN
MDR report key: 3770927
·
Received April 21, 2014
Report
- Report Number
- MW5035753
- Event Type
- Injury
- Date Received
- April 21, 2014
- Report Date
- April 20, 2014
- Manufacturer
- SIEMENS
- Product Code
- NSX
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- PA, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Description of Event or Problem · 1
PT HAD HYPOTENSION, CARDIAC ENZYMES WERE ORDERED STAT USING THE CPOE MACHINE. THE ORDER LAY IN THE RECIPIENT'S SILO, FOR AN HOUR BEFORE BEING CARRIED OUT DELAYING DIAGNOSIS. THERE IS NOT ANY WARNING THAT NEW ORDERS HAVE ARRIVED, UBIQUITOUSLY DELAYING CARE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 241670 | SOARIAN | CPOE | NSX | SIEMENS |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 89 YR | Hospitalization| L |