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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5119582 | 6145295 | I | 5119582-X | 20060916 | 20060929 | EXP | 2006112429 | PFIZER INC. | 73 | YR | F | N | 20060928 | OT | 20060501 | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5119582 | 1007725124 | PS | DETROL | 1 | (1 IN 1 D) | D | D | 20771 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5119582 | DE |
| 5119582 | DS |
| 5119582 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5119582 | BLINDNESS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5119582 | HP |
Therapies reported
| no results found |