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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6810001 | 7448775 | I | 6810001-1 | 20100623 | 20100630 | EXP | A0867538A | GLAXOSMITHKLINE | 54 | YR | M | Y | 20100630 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6810001 | 1014005722 | PS | AVANDIA | 1 | ORAL | 021071 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
6810001 | HO |
Reactions reported
Event ID | PT |
---|---|
6810001 | CARDIAC FAILURE CONGESTIVE |
6810001 | OEDEMA PERIPHERAL |
6810001 | RENAL FAILURE ACUTE |
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 |
---|---|---|---|---|---|
6810001 | 1014005722 | 20011101 | 20070912 |