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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6662501 | 7326166 | F | 6662501-5 | 20100325 | 20100331 | EXP | JP-MERCK-1003USA02775 | MERCK HUMAN HEALTH DIVISION | 78 | YR | F | Y | 20100401 | MD | JAPAN |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6662501 | 1013425047 | PS | JANUVIA | 1 | ORAL | ||||||
| 6662501 | 1013425048 | C | PROTHIADEN | 1 | ORAL | ||||||
| 6662501 | 1013425049 | C | LIVALO | 1 | ORAL | ||||||
| 6662501 | 1013425050 | C | SILECE | 2 | UNKNOWN | ||||||
| 6662501 | 1013425051 | C | EUGLUCON | 2 | ORAL | ||||||
| 6662501 | 1013425052 | C | EUGLUCON | 2 | ORAL | ||||||
| 6662501 | 1013425053 | C | LASIX | 1 | UNKNOWN |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6662501 | 1013425047 | DIABETES MELLITUS |
| 6662501 | 1013425051 | DIABETES MELLITUS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6662501 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6662501 | RENAL FAILURE ACUTE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6662501 | 1013425047 | 20091221 | 20100315 | 85 | DAY |
| 6662501 | 1013425051 | 20100301 | |||
| 6662501 | 1013425052 | 20091220 | |||
| 6662501 | 1013425053 | 20100301 |