MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2009-06-05 for * manufactured by .
[1266806]
Urine testing kit test positive for methadone opiates and chlamydia and others. Doctor refused to believe me that i don't use methadone on opiates and treat me for chlamydia until a confirmation test done for false reading. Doctor unable to give patient fair treatment because of false reading. There is no trust between patient and doctor. I want these test false reading removed from my medical record and destroy all false reading.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5011370 |
| MDR Report Key | 1400294 |
| Date Received | 2009-06-05 |
| Date of Event | 2009-05-05 |
| Date Added to Maude | 2009-06-16 |
| 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 | 0 |
| Initial Report to FDA | 0 |
| Report to FDA | 3 |
| Event Location | 0 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | * |
| Generic Name | URINE TESTING KIT |
| Product Code | MVO |
| Date Received | 2009-06-05 |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Hospitalization | 2009-06-05 |