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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6752492 | 7412504 | I | 6752492-0 | 20100101 | 20100601 | DIR | 53 | YR | M | N | 245 | LBS | 20100529 | OT | N | N | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6752492 | 1013796368 | PS | ACTOS | 1 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
6752492 | OT |
Reactions reported
Event ID | PT |
---|---|
6752492 | DYSPNOEA |
6752492 | WEIGHT INCREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |