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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4415390 | 4196472 | I | 4415390-3 | 20030801 | 20030904 | 20040630 | PER | 2003037446 | WWS PFIZER INC | N | 20040617 | MD |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4415390 | 1005076681 | PS | ZOLOFT | 1 | U | D | 19839 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4415390 | 1005076681 | DEPRESSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4415390 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 4415390 | CONVULSION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4415390 | CR |
| 4415390 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4415390 | 1005076681 | 20030601 |