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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6669378 | 7345867 | I | 6669378-2 | 20100405 | 20100406 | EXP | A0853538A | GLAXOSMITHKLINE | 52 | YR | M | Y | 119.1 | KG | 20100406 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6669378 | 1013452393 | PS | AVANDIA | 1 | ORAL | 4MG PER DAY | 021071 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
6669378 | HO |
Reactions reported
Event ID | PT |
---|---|
6669378 | CORONARY ARTERY DISEASE |
6669378 | MYOCARDIAL INFARCTION |
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 |
---|---|---|---|---|---|
6669378 | 1013452393 | 20050601 | 20070901 |