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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6671349 | 7347495 | F | 6671349-7 | 20100405 | 20100407 | EXP | A0804453A | GLAXOSMITHKLINE | 76 | YR | F | Y | 20100407 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6671349 | 1013459692 | PS | AVANDIA | 1 | ORAL | 4MG PER DAY | 021071 |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
6671349 | 1013459692 | TYPE 2 DIABETES MELLITUS |
Outcome of event
Event ID | OUTC COD |
---|---|
6671349 | HO |
Reactions reported
Event ID | PT |
---|---|
6671349 | CARDIAC VALVE DISEASE |
6671349 | CORONARY ARTERY DISEASE |
6671349 | MYOCARDIAL INFARCTION |
6671349 | TACHYCARDIA |
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 |
---|---|---|---|---|---|
6671349 | 1013459692 | 20050210 | 20060614 | 490 | DAY |