PARAGARD 380A Adverse Event: Device dislocation
PARAGARD 380A Adverse Event: Device dislocation is one of 4,500 adverse events in the FDATracker dataset. Key details — Primary drug: PARAGARD 380A; Product category: Drug; Primary reaction: Device dislocation.
| Primary drug | PARAGARD 380A |
|---|---|
| Product category | Drug |
| Primary reaction | Device dislocation |
| All reactions | Device dislocation; Dyspareunia |
| Seriousness | Serious |
| Patient outcome | Recovered/Resolved |
| Patient sex | Female |
| All drugs reported | PARAGARD 380A; PROTONIX |
| Reporter country | US |
| Reporter type | 3 |
| Report date | 20140312 |
| Report ID | 10004719 |
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