MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-03-13 for EUFLEXXA INJECTION ALTERNATIVE TO KNEE SURGERY manufactured by Ferring Pharmaceuticals, Inc..
[183885592]
Received euflexxa injection in left knee on (b)(6) 2020 and developed worsening joint pain in hands, left shoulder and back. Left knee feels the same pain and locks.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5093764 |
| MDR Report Key | 9834875 |
| Date Received | 2020-03-13 |
| Date of Report | 2020-03-12 |
| Date of Event | 2020-03-05 |
| Date Added to Maude | 2020-03-16 |
| 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 | 3 |
| Reporter Occupation | PATIENT |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | EUFLEXXA INJECTION ALTERNATIVE TO KNEE SURGERY |
| Generic Name | ACID, HYALURONIC, INTRAARTICULAR |
| Product Code | MOZ |
| Date Received | 2020-03-13 |
| Device Availability | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | FERRING PHARMACEUTICALS, INC. |
| Product Code | --- |
| Date Received | 2020-03-13 |
| Device Sequence No | 101 |
| Device Event Key | 0 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-03-13 |