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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6081342 | 6808818 | F | 6081342-3 | 20090216 | 20090218 | EXP | US-ASTRAZENECA-2008UW24628 | AZPRODUW00 | 96 | YR | F | Y | 20090218 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
6081342 | 1011141619 | PS | NEXIUM | 1 | ORAL | 021153 |
Indications of drugs used
no results found |
Outcome of event
Event ID | OUTC COD |
---|---|
6081342 | HO |
Reactions reported
Event ID | PT |
---|---|
6081342 | LOSS OF CONSCIOUSNESS |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |