MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-08-21 for RADIATION THERAPY manufactured by Unk.
[83210058]
Doctors from (b)(6) hospital corp used radiation to remove tonsils which later i developed tumors and cancer. Date of use: (b)(6) 1973. "how was it taken or used: oral. " the problem did not stop after the person reduced the dose or stopped taking or using the product.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5071697 |
| MDR Report Key | 6806782 |
| Date Received | 2017-08-21 |
| Date of Report | 2017-08-17 |
| Date of Event | 1973-03-18 |
| Date Added to Maude | 2017-08-21 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 0 |
| Reprocessed and Reused Flag | 0 |
| Reporter Occupation | PATIENT |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | RADIATION THERAPY |
| Generic Name | RADIATION THERAPY MEDICAL SYSTEM |
| Product Code | LHN |
| Date Received | 2017-08-21 |
| Device Availability | N |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 0 |
| Device Event Key | 0 |
| Manufacturer | UNK |
| Manufacturer Address | UNK UNK |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Hospitalization; 2. Deathisabilit | 2017-08-21 |