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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4465953 | 5664773 | I | 4465953-4 | 20040917 | 20040930 | EXP | S04-DEN-04699-01 | FOREST LABORATORIES INC. | 87 | YR | M | N | 20040928 | OT | 20040828 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4465953 | 1005264932 | PS | AKARIN (CITALOPRAM) | 2 | ORAL | 10 MG QD PO | D | D | 20822 | ||
| 4465953 | 1005287961 | SS | CORODIL (ENALAPRIL) | 2 | D | D | |||||
| 4465953 | 1005287963 | C | CENTYL MED KALIUMKLORID MITE 9BENDROFLUMETHIAZIDE) | 2 | D | D |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4465953 | 1005264932 | DEPRESSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4465953 | DE |
| 4465953 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4465953 | CONFUSIONAL STATE |
| 4465953 | DRUG INTERACTION |
| 4465953 | HYPONATRAEMIA |
| 4465953 | SYNCOPE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4465953 | FGN |
| 4465953 | HP |
| 4465953 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4465953 | 1005264932 | 20040826 | |||
| 4465953 | 1005287961 | 20040826 | |||
| 4465953 | 1005287963 | 20040828 |