MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2014-11-13 for RADIATION manufactured by .
[5231418]
Peg tube placement for grade 3 oral pain unlikely related the agent. Event happened during cycle 6. Suspect product: radiation. Dose, frequency and route used: 6000 cgy. Therapy dates: (b)(6) 2014.
Patient Sequence No: 1, Text Type: D, B5
Report Number | MW5039150 |
MDR Report Key | 4270321 |
Date Received | 2014-11-13 |
Date of Report | 2014-11-06 |
Date of Event | 2014-09-29 |
Date Added to Maude | 2014-11-24 |
Event Key | 0 |
Report Source Code | Voluntary report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 0 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Single Use | 0 |
Previous Use Code | 0 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | RADIATION |
Generic Name | RADIATION |
Product Code | KPQ |
Date Received | 2014-11-13 |
Device Sequence No | 1 |
Device Event Key | 0 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2014-11-13 |