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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6666849 | 7357834 | I | 6666849-X | 20090217 | 20100319 | 20100331 | EXP | 1000012760 | FOREST LABORATORIES, INC. | 75 | YR | F | N | 20100330 | OT | DENMARK |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6666849 | 1013442035 | PS | CITALOPRAM HYDROBROMIDE | 1 | ORAL | 30 MG (20 MG, 1 IN 1 D), ORAL | Y | D | 20822 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6666849 | 1013442035 | DEPRESSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6666849 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6666849 | TARDIVE DYSKINESIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6666849 | FGN |
| 6666849 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6666849 | 1013442035 | 20041213 | 20090306 |