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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5858736 | 6839621 | I | 5858736-1 | 20080705 | 20080711 | 20080818 | PER | WAES 0807USA02128 | MERCK + CO., INC. | 57 | YR | F | N | 20080815 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5858736 | 1010355561 | PS | JANUVIA | 1 | ORAL | 100 MG/DAILY/PO | Y | D | 21995 | ||
| 5858736 | 1010461217 | C | CORGARD | 1 | |||||||
| 5858736 | 1010461218 | C | LASIX | 1 | |||||||
| 5858736 | 1010461219 | C | CALCITRIOL | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5858736 | 1010355561 | DIABETES MELLITUS |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 5858736 | ABDOMINAL PAIN |
| 5858736 | BACK PAIN |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 5858736 | CR |
| 5858736 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 5858736 | 1010355561 | 20080703 | 20080709 |