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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6683578 | 7330275 | F | 6683578-7 | 20090409 | 20100406 | 20100413 | EXP | TCI2010A00626 | TAKEDA PHARMACEUTICALS NORTH AMERICA | 69 | YR | F | N | 20100412 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6683578 | 1013512199 | PS | ACTOS | 1 | ORAL | 7.5 MG (7.5 MG, 1 IN 1 D), ORAL | D | D | 21073 | ||
6683578 | 1013566280 | C | VENTANEURIN (PO) (FURSULTIAMINE, PYRIDOXAL 5- PHOSPHATE, HYDROXCOBA) | 2 | |||||||
6683578 | 1013566281 | C | DEPAS (ETIZOLAM) | 2 | |||||||
6683578 | 1013566282 | C | STAYBLA (IMIDAFENACIN) (UROLOGICALS) | 2 | |||||||
6683578 | 1013566286 | C | AMARYL | 1 | |||||||
6683578 | 1013566288 | C | DIOVAN | 1 | |||||||
6683578 | 1013566290 | C | AMLODIPINE BESYLATE | 1 | |||||||
6683578 | 1013566295 | C | TATSUPLAMIN (PRAVASTATIN SODIUM) | 2 | |||||||
6683578 | 1013566297 | C | LIVALO (ITAVASTATIN CALCIUM) | 2 | |||||||
6683578 | 1013566302 | C | FLUITRAN (TRICHLORMETHIZIDE) | 2 | |||||||
6683578 | 1013566305 | C | NORVASC | 1 | |||||||
6683578 | 1013566309 | C | PREMINENT (HYDROCHLOROTHIAZIDE, LOSARTAN POTASSIUM) | 2 | |||||||
6683578 | 1013566429 | C | CRESTOR | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6683578 | 1013512199 | DIABETES MELLITUS |
Outcome of event
Event ID | OUTC COD |
---|---|
6683578 | HO |
Reactions reported
Event ID | PT |
---|---|
6683578 | EYELID OEDEMA |
6683578 | LACUNAR INFARCTION |
6683578 | WHITE BLOOD CELL COUNT DECREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
6683578 | FGN |
6683578 | HP |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
6683578 | 1013512199 | 20090323 | 20090723 | 121 | DAY |