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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5659094 | 6531950 | F | 1 | 5659094-8 | 20070917 | 20071022 | 20080219 | PER | WAES 0709USA04071 | MERCK + CO., INC. | 68 | YR | M | N | 20080215 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5659094 | 1009627598 | PS | JANUVIA | 1 | ORAL | 100 MG/DAILY/PO | D | D | 21995 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5659094 | 1009627598 | TYPE 2 DIABETES MELLITUS |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 5659094 | BACK PAIN |
| 5659094 | FATIGUE |
| 5659094 | HEADACHE |
| 5659094 | PAIN IN EXTREMITY |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5659094 | CSM |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5659094 | 1009627598 | 20070917 |