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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4305203 | 4105688 | I | 4305203-2 | 20040101 | 20040115 | 20040223 | PER | SU-2004-002058 | SANKYO PHARMA INC. | N | 20040217 | MD |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4305203 | 1004655655 | PS | BENICAR | 1 | ORAL | MG UNK PO | U | U | 21286 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4305203 | 1004655655 | HYPERTENSION |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 4305203 | HYPERKALAEMIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4305203 | CR |
| 4305203 | HP |
Therapies reported
| no results found |