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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6664087 | 7341254 | I | 6664087-8 | 20100329 | 20100401 | EXP | A0852771A | GLAXOSMITHKLINE | 63 | YR | F | Y | 68.2 | KG | 20100401 | CN | 19990706 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6664087 | 1013430969 | PS | AVANDIA | 1 | ORAL | 4MG PER DAY | 021071 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
6664087 | DE |
6664087 | HO |
Reactions reported
Event ID | PT |
---|---|
6664087 | CORONARY ARTERY DISEASE |
6664087 | DEATH |
6664087 | DIABETES MELLITUS |
6664087 | PERIPHERAL VASCULAR DISORDER |
6664087 | RENAL DISORDER |
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 |
---|---|---|---|---|---|
6664087 | 1013430969 | 19990701 |