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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6768082 | 7418689 | I | 6768082-X | 20090501 | 20100601 | 20100614 | EXP | AU-GENENTECH-302700 | GNEFDAAERSPRD | 80 | YR | F | Y | 20100614 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6768082 | 1013859514 | PS | LUCENTIS | 1 | INTRAOCULAR | 0.05 ML, UNK | NOT REPORTED |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6768082 | 1013859514 | MACULAR DEGENERATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6768082 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6768082 | CEREBROVASCULAR ACCIDENT |
| 6768082 | MYOCARDIAL INFARCTION |
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 |
|---|---|---|---|---|---|
| 6768082 | 1013859514 | 20090201 |