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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6686098 | 7366610 | I | 6686098-9 | 20090310 | 20100407 | 20100414 | EXP | TCI2009A04361 | TAKEDA PHARMACEUTICALS NORTH AMERICA. | 76 | YR | F | N | 20100413 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6686098 | 1013523649 | PS | ACTOS | 1 | ORAL | 15 MG (15 MG,1 IN 1 D) PER ORAL | Y | D | 21073 | ||
6686098 | 1013571636 | C | BASEN OD (VOGLIBOSE) | 2 | |||||||
6686098 | 1013571637 | C | BIGUANDIES | 2 | |||||||
6686098 | 1013571638 | C | PARIET (RABEPROZOLE SODIUM) | 2 | |||||||
6686098 | 1013571639 | C | CRESTOR | 1 | |||||||
6686098 | 1013571641 | C | LOSARTAN POTASSIUM | 1 | |||||||
6686098 | 1013571642 | C | SULFONAMIDES, UREA DERIVATIVES | 2 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6686098 | 1013523649 | TYPE 2 DIABETES MELLITUS |
Outcome of event
Event ID | OUTC COD |
---|---|
6686098 | HO |
Reactions reported
Event ID | PT |
---|---|
6686098 | ANGER |
6686098 | ANXIETY |
6686098 | ATRIAL FIBRILLATION |
6686098 | BLOOD PRESSURE INCREASED |
6686098 | CARDIAC FAILURE CHRONIC |
6686098 | DECREASED APPETITE |
6686098 | PARANOIA |
6686098 | PSYCHIATRIC SYMPTOM |
6686098 | PULMONARY CONGESTION |
6686098 | WEIGHT DECREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
6686098 | FGN |
6686098 | HP |
6686098 | SDY |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
6686098 | 1013523649 | 20080331 | 20090420 | 384 | DAY |