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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7789286 | 8163563 | I | 7789286-3 | 20071001 | 20110923 | 20110930 | EXP | US-GLAXOSMITHKLINE-A0844999A | GLAXOSMITHKLINE | 68 | YR | M | Y | 20110930 | LW | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7789286 | 1017678319 | PS | AVANDIA | 1 | ORAL | 4MG TWICE PER DAY | 021071 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7789286 | 1017678319 | DIABETES MELLITUS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7789286 | DE |
| 7789286 | HO |
| 7789286 | DS |
Reactions reported
| Event ID | PT |
|---|---|
| 7789286 | AMNESIA |
| 7789286 | DEATH |
| 7789286 | OXYGEN SUPPLEMENTATION |
| 7789286 | MYOCARDIAL INFARCTION |
| 7789286 | ILL-DEFINED DISORDER |
| 7789286 | DISORIENTATION |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |