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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6758780 | 7415099 | I | 6758780-6 | 20100518 | 20100524 | 20100603 | EXP | TCI2010A01964 | TAKEDA PHARMACEUTICALS NORTH AMERICA. | 68 | YR | F | N | 20100602 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6758780 | 1013820007 | PS | ACTOS | 1 | ORAL | PER ORAL | D | 21073 | |||
| 6758780 | 1013837839 | SS | CANDESARTAN CILEXETIL | 1 | ORAL | PER ORAL, PER ORAL | D | ||||
| 6758780 | 1013837840 | SS | PRAVASTATIN SODIUM | 1 | ORAL | PER ORAL |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6758780 | 1013837840 | HYPOKALAEMIA |
| 6758780 | 1013837840 | RENAL FAILURE ACUTE |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6758780 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6758780 | HYPOKALAEMIA |
| 6758780 | RENAL FAILURE ACUTE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 6758780 | HP |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6758780 | 1013820007 | 20100414 | |||
| 6758780 | 1013837839 | 20100414 | |||
| 6758780 | 1013837840 | 20100414 |