SOLIRIS Adverse Event: Mineral supplementation
SOLIRIS Adverse Event: Mineral supplementation is one of 4,500 adverse events in the FDATracker dataset. Key details — Primary drug: SOLIRIS; Product category: Drug; Primary reaction: Mineral supplementation.
| Primary drug | SOLIRIS |
|---|---|
| Product category | Drug |
| Primary reaction | Mineral supplementation |
| All reactions | Mineral supplementation; Haemoglobin decreased; Dyspnoea; Musculoskeletal stiffness; Fatigue |
| Seriousness | Serious |
| Patient outcome | Unknown |
| Patient sex | Female |
| All drugs reported | SOLIRIS |
| Reporter country | US |
| Reporter type | 5 |
| Report date | 20140313 |
| Report ID | 10005962 |
$299/mo
Try FDATracker →