MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-07-31 for DRUG TEST REF# 6576843-0438 manufactured by Unk.
[115909601]
I took a drug test, and it came up as? Positive? For fentanyl. Thank god, my doctor and staff realized it was myrbetriq showing a false positive as fentanyl. They were looking at me as if i was a drug addict. Might want to put a warning on the box or send out notices to all drs. Myrbetriq? Overactive bladder medicine -- shows up as fentanyl on a drug test. Thank you, (b)(6).
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5078757 |
| MDR Report Key | 7739372 |
| Date Received | 2018-07-31 |
| Date of Report | 2018-07-28 |
| Date of Event | 2018-07-20 |
| Date Added to Maude | 2018-08-01 |
| 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 | 3 |
| 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 | DRUG TEST |
| Generic Name | ENZYME, IMMUNOASSAY |
| Product Code | DJG |
| Date Received | 2018-07-31 |
| Model Number | REF# 6576843-0438 |
| Device Availability | Y |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | UNK |
| Manufacturer Address | UNK UNK |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2018-07-31 |