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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6664028 | 7161996 | F | 6664028-3 | 20100329 | 20100401 | EXP | A0813837A | GLAXOSMITHKLINE | 56 | YR | M | Y | 84.1 | KG | 20100401 | CN | 20070723 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6664028 | 1013430841 | PS | AVANDIA | 1 | ORAL | 4MG PER DAY | 021071 | ||||
| 6664028 | 1013430842 | C | NORVASC | 1 | |||||||
| 6664028 | 1013430843 | C | LEVITRA | 1 | |||||||
| 6664028 | 1013430844 | C | VIAGRA | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6664028 | 1013430841 | DIABETES MELLITUS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6664028 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 6664028 | CORONARY ARTERY DISEASE |
| 6664028 | GENERAL PHYSICAL HEALTH DETERIORATION |
| 6664028 | SUDDEN CARDIAC DEATH |
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 |
|---|---|---|---|---|---|
| 6664028 | 1013430841 | 20030901 | 20070701 |