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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5577646 | 6517032 | I | 5577646-0 | 20071219 | 20071225 | 20071231 | EXP | PHBS2007JP21381 | NOVARTIS PHARMACEUTICALS CORP. | 75 | YR | M | Y | 20071229 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5577646 | 1009349375 | PS | DIOVAN | 1 | ORAL | 160 MG/DAY | 020665 | ||||
| 5577646 | 1009349376 | C | ACTOS | 1 | ORAL | 15 MG/DAY |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5577646 | 1009349375 | HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5577646 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 5577646 | SUDDEN DEATH |
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 |
|---|---|---|---|---|---|
| 5577646 | 1009349375 | 20070711 | 20071219 | 162 | DAY |
| 5577646 | 1009349376 | 20060426 | 20071219 | 603 | DAY |