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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5798416 | 6661383 | F | 1 | 5798416-4 | 20071101 | 20080616 | 20080630 | EXP | 000772 | OTSUKA PHARMACEUTICAL | 66 | YR | M | N | 20080627 | GERMANY |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5798416 | 1010123825 | PS | PLETAL | 1 | ORAL | 100 MG, BID; ORAL | D | D | 20863 | ||
| 5798416 | 1010163574 | C | SIMVASTATIN | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5798416 | 1010123825 | INTERMITTENT CLAUDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5798416 | DS |
| 5798416 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5798416 | APHASIA |
| 5798416 | DISTURBANCE IN ATTENTION |
| 5798416 | DYSARTHRIA |
| 5798416 | DYSPHAGIA |
| 5798416 | FACIAL PARESIS |
| 5798416 | HEMIPLEGIA |
| 5798416 | ISCHAEMIC STROKE |
| 5798416 | VASCULAR OCCLUSION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5798416 | HP |
| 5798416 | SDY |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5798416 | 1010123825 | 20070417 | 20071101 |