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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5526580 | 6475249 | I | 5526580-0 | 20071112 | 20071127 | EXP | DE-AMGEN-US253594 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5526580 | 1009196718 | PS | ENBREL | 1 | NOT PROVIDED |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5526580 | 1009196718 | ANKYLOSING SPONDYLITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5526580 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5526580 | CROHN'S DISEASE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |