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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6815086 | 7455039 | I | 6815086-4 | 20100405 | 20100630 | DIR | 59 | YR | F | N | 238 | LBS | 20100629 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6815086 | 1014027147 | PS | ACTOS | 1 | ORAL | 30 MG QD PO | N |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6815086 | 1014027147 | TYPE 2 DIABETES MELLITUS |
Outcome of event
Event ID | OUTC COD |
---|---|
6815086 | OT |
Reactions reported
Event ID | PT |
---|---|
6815086 | LYMPHOEDEMA |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
6815086 | 1014027147 | 20091201 | 20100410 | 4 | MON |