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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5798419 | 6697733 | I | 5798419-X | 20080301 | 20080616 | 20080630 | EXP | 001441 | OTSUKA PHARMACEUTICAL | 85 | YR | F | N | 20080627 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5798419 | 1010123836 | PS | PLETAL | 1 | ORAL | 100 MG, BID; ORAL | N | D | 20863 | ||
| 5798419 | 1010163757 | C | ASPIRIN | 1 | |||||||
| 5798419 | 1010163758 | C | ARB (ARB) | 2 | |||||||
| 5798419 | 1010163759 | C | DIURETICS | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5798419 | 1010123836 | ARTERIOSCLEROSIS OBLITERANS |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 5798419 | DIALYSIS |
| 5798419 | RENAL FAILURE ACUTE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5798419 | HP |
| 5798419 | SDY |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5798419 | 1010123836 | 20080201 | 20080322 | 51 | DAY |