Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8248787 | 8486006 | I | 8248787-4 | 20110728 | 20120323 | 20120331 | EXP | DE-ALLERGAN-1117173US | ALLERGANFDA | 82 | YR | F | Y | 20120331 | MD | GERMANY |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8248787 | 1019282891 | PS | OZURDEX | 1 | INTRAOCULAR | 0.7 MG, SINGLE | 022315 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8248787 | 1019282891 | MACULAR OEDEMA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8248787 | DS |
Reactions reported
| Event ID | PT |
|---|---|
| 8248787 | BLINDNESS UNILATERAL |
| 8248787 | GLAUCOMA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 8248787 | 1019282891 | 20110412 | 20110412 | 1 | DAY |