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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6696853 | 7374787 | I | 6696853-7 | 20100415 | 20100422 | EXP | TUK2010A00054 | TAKEDA PHARMACEUTICALS NORTH AMERICA. | 54 | YR | F | N | 20100421 | UNITED KINGDOM |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6696853 | 1013569006 | PS | ACTOS | 1 | ORAL | (15 MG) ORAL | Y | 21073 | |||
6696853 | 1013615149 | C | METFORMIN HCL | 1 | |||||||
6696853 | 1013615150 | C | NAPROXEN | 1 | |||||||
6696853 | 1013615151 | C | SIMVASTATIN | 1 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6696853 | 1013569006 | DIABETES MELLITUS |
Outcome of event
Event ID | OUTC COD |
---|---|
6696853 | OT |
6696853 | RI |
Reactions reported
Event ID | PT |
---|---|
6696853 | ARTHRALGIA |
6696853 | HYPOAESTHESIA |
6696853 | JOINT SWELLING |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
6696853 | FGN |
6696853 | HP |
6696853 | OTH |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
6696853 | 1013569006 | 20091104 | 20100320 | 136 | DAY |