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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7582993 | 8016561 | I | 7582993-7 | 20110617 | 20110630 | EXP | CA-GENENTECH-320608 | GNEFDAAERSPRD | YR | F | Y | 20110630 | CN | SWITZERLAND |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7582993 | 1016902964 | PS | LUCENTIS | 1 | INTRAOCULAR | 0.5 MG, UNK | NOTREPORTED |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7582993 | 1016902964 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7582993 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7582993 | BLINDNESS UNILATERAL |
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 |
|---|---|---|---|---|---|
| 7582993 | 1016902964 | 20100101 |