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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6664020 | 6999712 | F | 6664020-9 | 20100329 | 20100401 | EXP | A0785196A | GLAXOSMITHKLINE | 63 | YR | F | Y | 20100401 | MD | 20070603 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6664020 | 1013430823 | PS | AVANDIA | 1 | ORAL | 4MG TWICE PER DAY | 021071 | ||||
6664020 | 1013430824 | SS | AVANDAMET | 1 | ORAL | 021410 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6664020 | 1013430823 | DRUG USE FOR UNKNOWN INDICATION |
6664020 | 1013430824 | DIABETES MELLITUS |
Outcome of event
Event ID | OUTC COD |
---|---|
6664020 | DE |
6664020 | HO |
Reactions reported
Event ID | PT |
---|---|
6664020 | CARDIAC FAILURE CONGESTIVE |
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 |
---|---|---|---|---|---|
6664020 | 1013430823 | 20030601 | 20070524 | ||
6664020 | 1013430824 | 20050901 | 20050901 |