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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5464602 | 6457933 | I | 5464602-6 | 20070101 | 20070516 | 20070820 | PER | WAES 0705USA03093 | MERCK + CO., INC. | N | 20070816 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5464602 | 1008961555 | PS | JANUVIA | 1 | ORAL | 100 MG/DAILY/PO | Y | D | 21995 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5464602 | 1008961555 | TYPE 2 DIABETES MELLITUS |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 5464602 | DIZZINESS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5464602 | CR |
| 5464602 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5464602 | 1008961555 | 20070101 | 20070101 |