MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2013-04-11 for NARROW BAND UVB manufactured by .
[3252597]
(b)(6). I have appointment to see dr (b)(6) on (b)(6) 2013, 10:45 a. M. At (b)(6). The reason for doctor visit is therapy narrow band u ub only. Therapy 3 times a week for 3 months referred by dr (b)(6). Any question about therapy please call dr (b)(6). Two types of medication given by dr (b)(6) are good. Four days after i used those medicines i start feeling better, but the itching still bothers me and wakes me up at night. I last night tried to use benadryl extra strength, it reduced the itching. Thank dr (b)(6) to help me get out of severe symptoms. I hope everything might go away faster after therapy has been done.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5029735 |
| MDR Report Key | 3060056 |
| Date Received | 2013-04-11 |
| Date of Report | 2013-04-09 |
| Date Added to Maude | 2013-04-17 |
| 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 |
| 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 |
| Generic Name | NARROW BAND UVB |
| Product Code | ILY |
| Date Received | 2013-04-11 |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2013-04-11 |