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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6713624 | 7379269 | F | 6713624-3 | 20100430 | 20100506 | EXP | A0857811A | GLAXOSMITHKLINE | YR | M | Y | 127.3 | KG | 20100506 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6713624 | 1013638433 | PS | AVANDIA | 1 | ORAL | 4MG PER DAY | 021071 | ||||
6713624 | 1013638434 | SS | ACTOS | 1 | ORAL |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
6713624 | HO |
Reactions reported
Event ID | PT |
---|---|
6713624 | ARRHYTHMIA |
6713624 | ATRIOVENTRICULAR BLOCK |
6713624 | CARDIAC FAILURE CONGESTIVE |
6713624 | DRUG HYPERSENSITIVITY |
6713624 | FLUID RETENTION |
6713624 | RASH |
6713624 | SWELLING |
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 |
---|---|---|---|---|---|
6713624 | 1013638433 | 19990101 | 20000723 |