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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5468712 | 6451749 | I | 5468712-9 | 20070619 | 20070820 | PER | WAES 0706USA03791 | MERCK + CO., INC. | F | N | 20070816 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5468712 | 1008976316 | PS | JANUVIA | 1 | ORAL | 100 MG, DAILY; PO | D | D | 21995 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5468712 | 1008976316 | DIABETES MELLITUS |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
5468712 | DIARRHOEA |
5468712 | NAUSEA |
5468712 | VOMITING |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
5468712 | CR |
5468712 | HP |
Therapies reported
no results found |