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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6690552 | 7061290 | F | 6690552-3 | 20100419 | 20100421 | EXP | A0775978A | GLAXOSMITHKLINE | 68 | YR | F | Y | 81.8 | KG | 20100421 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6690552 | 1013542183 | PS | AVANDIA | 1 | ORAL | 1TAB TWICE PER DAY | 021071 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
6690552 | HO |
Reactions reported
Event ID | PT |
---|---|
6690552 | CARDIAC FAILURE CONGESTIVE |
6690552 | CARDIOVASCULAR DISORDER |
6690552 | CONDITION AGGRAVATED |
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 |
---|---|---|---|---|---|
6690552 | 1013542183 | 20030101 | 20080901 |