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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5659095 | 6522433 | F | 1 | 5659095-X | 20071023 | 20080219 | PER | WAES 0710USA00025 | MERCK + CO., INC. | M | N | 20080215 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5659095 | 1009627599 | PS | JANUVIA | 1 | ORAL | 50 MG/PO | Y | D | 21995 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5659095 | 1009627599 | BLOOD GLUCOSE |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 5659095 | BLOOD CREATININE INCREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5659095 | CR |
| 5659095 | HP |
Therapies reported
| no results found |