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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6660447 | 7338493 | I | 6660447-X | 20100329 | 20100329 | 20100331 | EXP | JP-SANOFI-AVENTIS-2010SA018106 | SANOFI-AVENTIS | Y | 20100331 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6660447 | 1013416638 | PS | AMARYL | 1 | UNK | 020496 | |||||
6660447 | 1013416639 | C | PIOGLITAZONE | 1 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
6660447 | OT |
Reactions reported
Event ID | PT |
---|---|
6660447 | THROMBOCYTOPENIC PURPURA |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |