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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7919974 | 8257126 | I | 7919974-7 | 20111104 | 20111115 | EXP | TPA2011A07345 | TAKEDA PHARMACEUTICALS NORTH AMERICA. | YR | M | N | 20111114 | CN | UNITED STATES |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7919974 | 1018068380 | PS | ACTOS | 1 | U | U | 021073 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7919974 | 1018068380 | DIABETES MELLITUS |
Outcome of event
Event ID | OUTC COD |
---|---|
7919974 | OT |
7919974 | RI |
Reactions reported
Event ID | PT |
---|---|
7919974 | BLADDER CANCER |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
7919974 | CSM |
7919974 | CR |
Therapies reported
no results found |