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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6688677 | 7167779 | F | 6688677-1 | 20100419 | 20100420 | EXP | A0814615A | GLAXOSMITHKLINE | 46 | YR | M | Y | 56.8 | KG | 20100420 | CN | 20080123 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6688677 | 1013534075 | PS | AVANDIA | 1 | ORAL | 8MG UNKNOWN | 021071 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
6688677 | DE |
6688677 | HO |
Reactions reported
Event ID | PT |
---|---|
6688677 | CONDITION AGGRAVATED |
6688677 | DEATH |
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 |
---|---|---|---|---|---|
6688677 | 1013534075 | 20080123 |