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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6696283 | 7338493 | F | 6696283-8 | 20100329 | 20100421 | 20100426 | EXP | JP-SANOFI-AVENTIS-2010SA018106 | SANOFI-AVENTIS | YR | Y | 20100426 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6696283 | 1013566363 | PS | AMARYL | 1 | UNK | 20496 | |||||
| 6696283 | 1013566364 | SS | ACTOS | 1 | |||||||
| 6696283 | 1013566365 | SS | TAKEPRON | 2 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6696283 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6696283 | THROMBOCYTOPENIC PURPURA |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |