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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 7491960 | 7970787 | I | 7491960-3 | 20101001 | 20110518 | DIR | 59 | YR | M | N | 20110517 | PH | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 7491960 | 1016543432 | PS | GKUOUZUDE 5 MG TEVA | 2 | ORAL | 5 MG 2 AM 1 PM PO | Y | D |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 7491960 | 1016543432 | DIABETES MELLITUS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 7491960 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 7491960 | BLOOD GLUCOSE INCREASED |
| 7491960 | PRODUCT SUBSTITUTION ISSUE |
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 |
|---|---|---|---|---|---|
| 7491960 | 1016543432 | 20100908 | 20101007 |