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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6740180 | 7062120 | F | 6740180-6 | 20100519 | 20100525 | EXP | A0789309A | GLAXOSMITHKLINE | 57 | YR | F | Y | 61.4 | KG | 20100525 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6740180 | 1013747240 | PS | AVANDIA | 1 | ORAL | 4MG PER DAY | 021071 | ||||
| 6740180 | 1013747241 | C | ASPIRIN | 1 | |||||||
| 6740180 | 1013747242 | C | PLAVIX | 1 | |||||||
| 6740180 | 1013747243 | C | GLUCOPHAGE | 1 | |||||||
| 6740180 | 1013747244 | C | NORVASC | 1 | |||||||
| 6740180 | 1013747245 | C | DAYPRO | 1 | |||||||
| 6740180 | 1013747246 | C | ALTACE | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6740180 | 1013747240 | DIABETES MELLITUS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6740180 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6740180 | CARDIAC FAILURE CONGESTIVE |
| 6740180 | CORONARY ARTERY DISEASE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |