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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6753028 | 7413586 | I | 6753028-0 | 20100602 | DIR | YR | F | N | 134 | LBS | 20100207 | N | N | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6753028 | 1013798291 | PS | NEXIUM | 1 | 1 A DAY | N | |||||
| 6753028 | 1013829043 | SS | ACTOS | 1 | 1 A DAY | N |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6753028 | 1013829043 | DIABETES MELLITUS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6753028 | DE |
Reactions reported
| Event ID | PT |
|---|---|
| 6753028 | MYOCARDIAL INFARCTION |
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 |
|---|---|---|---|---|---|
| 6753028 | 1013798291 | 3 | YR | ||
| 6753028 | 1013829043 | 1 | YR |