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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5705912 | 6613834 | F | 1 | 5705912-4 | 19980101 | 20080326 | 20080411 | EXP | S08-NOR-01144-01 | FOREST LABORATORIES INC. | 20 | YR | F | N | 20080409 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5705912 | 1009789053 | PS | CITALOPRAM HYDROBROMIDE | 1 | ORAL | 20 MG QD PO | D | 20822 | |||
| 5705912 | 1009833958 | SS | TRIPHASIL-21 | 1 | D | D | |||||
| 5705912 | 1009833959 | SS | IMOVANE (ZOPICLONE) | 2 | 20822 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5705912 | 1009789053 | DEPRESSION |
| 5705912 | 1009833958 | CONTRACEPTION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5705912 | HO |
| 5705912 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5705912 | ABNORMAL BEHAVIOUR |
| 5705912 | ANXIETY |
| 5705912 | DEPRESSION |
| 5705912 | DRUG ABUSE |
| 5705912 | DRUG INTOLERANCE |
| 5705912 | MENTAL DISORDER |
| 5705912 | POISONING |
| 5705912 | PSYCHOTIC DISORDER |
| 5705912 | SCHIZOID PERSONALITY DISORDER |
| 5705912 | SOCIAL PHOBIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5705912 | FGN |
| 5705912 | HP |
| 5705912 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5705912 | 1009789053 | 19981120 | 19990601 |