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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6694707 | 7154411 | F | 6694707-3 | 20100420 | 20100423 | EXP | A0812500A | GLAXOSMITHKLINE | 39 | YR | F | Y | 20100423 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6694707 | 1013559261 | PS | AVANDIA | 1 | ORAL | 4MG TWICE PER DAY | 021071 | ||||
| 6694707 | 1013559262 | SS | AVANDAMET | 1 | ORAL | 021410 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6694707 | 1013559261 | DIABETES MELLITUS |
| 6694707 | 1013559262 | DIABETES MELLITUS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6694707 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6694707 | CARDIAC DISORDER |
| 6694707 | CARDIAC FAILURE CONGESTIVE |
| 6694707 | CARDIOMYOPATHY |
| 6694707 | HYPERTENSION |
| 6694707 | MYOCARDIAL ISCHAEMIA |
| 6694707 | WEIGHT INCREASED |
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 |
|---|---|---|---|---|---|
| 6694707 | 1013559261 | 20010601 | 20070701 | ||
| 6694707 | 1013559262 | 20010601 | 20070701 |