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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6450924 | 7011146 | F | 6450924-9 | 20060601 | 20091117 | 20091123 | EXP | A0788369A | GLAXOSMITHKLINE | 47 | M | Y | 20091123 | CN | 20080610 | UNITED STATES |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6450924 | 1012625478 | PS | AVANDIA | 1 | ORAL | 021071 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6450924 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 6450924 | CARDIAC FAILURE |
| 6450924 | DEATH |
| 6450924 | INJURY |
| 6450924 | MYOCARDIAL INFARCTION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6450924 | 1012625478 | 20071201 |