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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6702251 | 7235417 | F | 6702251-X | 20091224 | 20100420 | 20100429 | EXP | JP-MERCK-0912USA03605 | MERCK HUMAN HEALTH DIVISION | 60 | YR | M | Y | 69 | KG | 20100429 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6702251 | 1013593378 | PS | JANUVIA | 1 | ORAL | 21995 | |||||
| 6702251 | 1013593379 | SS | AMARYL | 1 | ORAL | ||||||
| 6702251 | 1013593380 | SS | ACTOS | 1 | ORAL | ||||||
| 6702251 | 1013593381 | SS | LIPITOR | 1 | ORAL | ||||||
| 6702251 | 1013593382 | SS | BASEN | 2 | ORAL |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6702251 | 1013593378 | TYPE 2 DIABETES MELLITUS |
| 6702251 | 1013593381 | HYPERCHOLESTEROLAEMIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6702251 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 6702251 | HYPERKALAEMIA |
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 |
|---|---|---|---|---|---|
| 6702251 | 1013593378 | 20091122 | 20091225 | 34 | DAY |
| 6702251 | 1013593379 | 20060101 | |||
| 6702251 | 1013593380 | 20060101 | |||
| 6702251 | 1013593381 | 20091005 | |||
| 6702251 | 1013593382 | 20060101 |