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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5526582 | 6475251 | I | 5526582-4 | 20071112 | 20071127 | EXP | DE-AMGEN-US253593 | 039976196:01 | Y | 20071127 | GERMANY |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5526582 | 1009196720 | PS | ENBREL | 1 | NOT PROVIDED |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5526582 | 1009196720 | ANKYLOSING SPONDYLITIS |
Outcome of event
Event ID | OUTC COD |
---|---|
5526582 | OT |
Reactions reported
Event ID | PT |
---|---|
5526582 | COLITIS ULCERATIVE |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |