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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5050538 | 6090755 | I | 5050538-1 | 20060101 | 20060628 | 20060707 | EXP | FRWYE859028JUN06 | WYETH PHARMACEUTICALS INC. | F | N | 20060706 | OT | FRANCE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5050538 | 1007463833 | PS | EFFEXOR | 1 | ORAL | 75 MG TOTAL DAILY | D | D | 20151 | ||
| 5050538 | 1007485989 | SS | ANXIOLYTICS (ANXIOLYTICS, , 0) | 2 | ORAL | D | D |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5050538 | 1007463833 | GENERALISED ANXIETY DISORDER |
| 5050538 | 1007485989 | GENERALISED ANXIETY DISORDER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5050538 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 5050538 | ANXIETY |
| 5050538 | COMPLETED SUICIDE |
| 5050538 | DRUG INEFFECTIVE |
| 5050538 | INSOMNIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5050538 | FGN |
| 5050538 | HP |
| 5050538 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5050538 | 1007463833 | 20060101 |