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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6758391 | 7423892 | I | 6758391-2 | 20100524 | 20100603 | EXP | TPA2010A03063 | TAKEDA PHARMACEUTICALS NORTH AMERICA. | YR | F | N | 20100602 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6758391 | 1013818616 | PS | ACTOS | 1 | U | U | 21073 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
6758391 | OT |
6758391 | RI |
Reactions reported
Event ID | PT |
---|---|
6758391 | BLADDER CANCER |
Reporting Sources (this data is often not reported and may therefore be missing here)
Event ID | RPSR COD |
---|---|
6758391 | CR |
6758391 | HP |
Therapies reported
no results found |