REBIF Adverse Event: Loss of consciousness
REBIF Adverse Event: Loss of consciousness is one of 4,500 adverse events in the FDATracker dataset. Key details — Primary drug: REBIF; Product category: Drug; Primary reaction: Loss of consciousness.
| Primary drug | REBIF |
|---|---|
| Product category | Drug |
| Primary reaction | Loss of consciousness |
| All reactions | Loss of consciousness; Fall; Gait disturbance; Convulsion; Influenza |
| Seriousness | Serious |
| Patient outcome | Unknown |
| Patient sex | Female |
| All drugs reported | REBIF; ZOLOFT /01011401/; COMPAZINE /00013302/; OXYCODONE |
| Reporter country | US |
| Reporter type | 5 |
| Report date | 20140312 |
| Report ID | 10003589 |
$299/mo
Try FDATracker →