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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8135839 | 8405113 | I | 8135839-2 | 20081228 | 20110617 | 20120214 | EXP | US-GLAXOSMITHKLINE-A0935766A | GLAXOSMITHKLINE | 51 | YR | M | Y | 20120214 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8135839 | 1018858276 | SS | AVANDAMET | 1 | ORAL | 021410 | |||||
| 8135839 | 1018858275 | PS | AVANDIA | 1 | ORAL | 4MG TWICE PER DAY | 021071 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8135839 | 1018858276 | DIABETES MELLITUS |
| 8135839 | 1018858275 | DIABETES MELLITUS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8135839 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 8135839 | CEREBROVASCULAR ACCIDENT |
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 |
|---|---|---|---|---|---|
| 8135839 | 1018858276 | 20031203 | 20071221 | ||
| 8135839 | 1018858275 | 20031203 | 20071221 |