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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5654710 | 6679160 | I | 5654710-9 | 20071022 | 20080219 | PER | WAES 0710USA04739 | MERCK + CO., INC. | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5654710 | 1009612028 | PS | JANUVIA | 1 | ORAL | PO | U | D | 21995 |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
5654710 | OEDEMA |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
5654710 | CR |
5654710 | HP |
Therapies reported
no results found |