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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6679632 | 7353608 | F | 6679632-6 | 20100412 | 20100413 | EXP | A0807534A | GLAXOSMITHKLINE | 60 | YR | M | Y | 20100413 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6679632 | 1013494299 | PS | AVANDIA | 1 | ORAL | 4MG TWICE PER DAY | 021071 | ||||
6679632 | 1013494300 | SS | AVANDARYL | 1 | ORAL | 021700 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
6679632 | HO |
Reactions reported
Event ID | PT |
---|---|
6679632 | INJURY |
6679632 | 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 |
---|---|---|---|---|---|
6679632 | 1013494299 | 20050801 | 20070401 | ||
6679632 | 1013494300 | 20070101 | 20070101 |