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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6252169 | 7038219 | I | 6252169-4 | 20080603 | 20090415 | 20090630 | EXP | US-GENENTECH-282225 | GNEFDAAERSPRD | 90 | F | Y | 20090630 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6252169 | 1011820327 | PS | LUCENTIS | 1 | INTRAOCULAR | 0.5 MG, Q4W | NOT REPORTED | ||||
| 6252169 | 1011820328 | C | ASPIRIN | 2 | |||||||
| 6252169 | 1011820329 | C | LEVOXYL | 1 | |||||||
| 6252169 | 1011820330 | C | ASPIRIN | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6252169 | 1011820327 | MACULAR DEGENERATION |
| 6252169 | 1011820328 | DRUG USE FOR UNKNOWN INDICATION |
| 6252169 | 1011820329 | DRUG USE FOR UNKNOWN INDICATION |
| 6252169 | 1011820330 | DRUG USE FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6252169 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6252169 | VISUAL ACUITY REDUCED |
| 6252169 | VITREOUS DETACHMENT |
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 |
|---|---|---|---|---|---|
| 6252169 | 1011820327 | 20080311 |