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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6316543 | 7078373 | F | 6316543-X | 20090709 | 20090810 | 20090820 | EXP | JP-GENENTECH-288221 | GNEFDAAERSPRD | 84 | M | Y | 20090820 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6316543 | 1012078071 | PS | LUCENTIS | 1 | INTRAOCULAR | 0.05 ML, UNK | NOT REPORTED |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6316543 | 1012078071 | MACULAR DEGENERATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6316543 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6316543 | SUBDURAL HAEMATOMA |
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 |
|---|---|---|---|---|---|
| 6316543 | 1012078071 | 20090708 |