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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6666845 | 7395835 | I | 6666845-2 | 20081122 | 20100318 | 20100331 | EXP | DSJ-2010-04496 | DAIICHI SANKYO INC. | 58 | YR | M | N | 20100326 | CN | BRAZIL |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6666845 | 1013442031 | PS | AMLODIPINE BESYLATE AND OLMESARTAN MEDOXOMIL | 1 | ORAL | 20/5 MG (1 IN 1D), PER ORAL | D | D | 22100 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6666845 | 1013442031 | HYPERTENSION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6666845 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6666845 | CEREBROVASCULAR ACCIDENT |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6666845 | CSM |
| 6666845 | FGN |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6666845 | 1013442031 | 20080101 | 20090101 |