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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7387794 | 7880768 | I | 7387794-0 | 20110103 | 20110316 | 20110331 | EXP | GB-GENENTECH-315620 | GNEFDAAERSPRD | 72 | YR | F | Y | 20110331 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7387794 | 1016144061 | PS | LUCENTIS | 1 | INTRAOCULAR | UNK DF, UNKNOWN | NOTREPORTED |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7387794 | 1016144061 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7387794 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 7387794 | DEATH |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |