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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5039982 | 6054776 | F | 5039982-6 | 20060522 | 20060524 | 20060630 | EXP | 2006AP02346 | AZPRODUW00 | 66 | YR | M | Y | 20060630 | MD | 20060522 | JAPAN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5039982 | 1007429042 | PS | TENORMIN | 1 | ORAL | 18240 | |||||
| 5039982 | 1007429043 | SS | DIOVAN | 1 | ORAL | 15 TABLETS | |||||
| 5039982 | 1007429044 | SS | CALBLOCK | 2 | ORAL | 15 TABLETS |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5039982 | 1007429043 | COMPLETED SUICIDE |
| 5039982 | 1007429044 | COMPLETED SUICIDE |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5039982 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 5039982 | COMPLETED SUICIDE |
| 5039982 | DRUG LEVEL ABOVE THERAPEUTIC |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5039982 | 1007429043 | 20060522 | 20060522 | 0 | DAY |
| 5039982 | 1007429044 | 20060522 | 20060522 | 0 | DAY |