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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6672938 | 7348721 | F | 6672938-6 | 20100405 | 20100408 | EXP | A0804458A | GLAXOSMITHKLINE | 76 | YR | M | Y | 136.4 | KG | 20100408 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6672938 | 1013466792 | PS | AVANDIA | 1 | ORAL | 8MG PER DAY | 021071 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
6672938 | OT |
Reactions reported
Event ID | PT |
---|---|
6672938 | CARDIAC FAILURE CONGESTIVE |
6672938 | CORONARY ARTERY DISEASE |
6672938 | ILL-DEFINED DISORDER |
6672938 | OEDEMA PERIPHERAL |
6672938 | PAIN |
6672938 | PLEURAL EFFUSION |
6672938 | PULMONARY OEDEMA |
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 |
---|---|---|---|---|---|
6672938 | 1013466792 | 20050706 | 20070601 | 696 | DAY |