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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5469480 | 6460318 | I | 5469480-7 | 20070504 | 20070820 | PER | WAES 0705USA01298 | MERCK HUMAN HEALTH DIVISION | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5469480 | 1008979187 | PS | JANUVIA | 1 | ORAL | PO | D | D | 21995 | ||
5469480 | 1009092555 | C | THERAPY UNSPECIFIED | 2 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5469480 | 1008979187 | TYPE 2 DIABETES MELLITUS |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
5469480 | ALOPECIA |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
5469480 | CR |
5469480 | HP |
Therapies reported
no results found |