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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7116576 | 7678662 | I | 7116576-X | 20101115 | 20101122 | EXP | A0893881A | GLAXOSMITHKLINE | YR | F | Y | 20101122 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7116576 | 1015164568 | PS | AVANDIA | 1 | ORAL | 021071 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
7116576 | 1015164568 | DIABETES MELLITUS |
Outcome of event
Event ID | OUTC COD |
---|---|
7116576 | DE |
Reactions reported
Event ID | PT |
---|---|
7116576 | SUDDEN CARDIAC DEATH |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |