LUCENTIS Adverse Event: Dysphagia
LUCENTIS Adverse Event: Dysphagia is one of 4,500 adverse events in the FDATracker dataset. Key details — Primary drug: LUCENTIS; Product category: Drug; Primary reaction: Dysphagia.
| Primary drug | LUCENTIS |
|---|---|
| Product category | Drug |
| Primary reaction | Dysphagia |
| All reactions | Dysphagia; Muscle contractions involuntary; Dysarthria |
| Seriousness | Serious |
| Patient outcome | Not Recovered/Not Resolved |
| Patient sex | Male |
| All drugs reported | LUCENTIS; KARDEGIC; BISOPROLOL; RILUTEK |
| Reporter country | FR |
| Reporter type | 3 |
| Report date | 20140313 |
| Report ID | 10005551 |
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