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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5470798 | 6429791 | I | 5470798-2 | 20070807 | 20070918 | 20070928 | EXP | US-AMGEN-QUU243915 | 039976196:01 | F | Y | 72.6 | KG | 20070928 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5470798 | 1008984043 | PS | ENBREL | 1 | SUBCUTANEOUS | P078155 | |||||
| 5470798 | 1008984044 | SS | ENBREL | 1 | P078155 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5470798 | 1008984043 | RHEUMATOID ARTHRITIS |
| 5470798 | 1008984044 | ANKYLOSING SPONDYLITIS |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5470798 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 5470798 | INJECTION SITE PAIN |
| 5470798 | RHEUMATOID ARTHRITIS |
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 |
|---|---|---|---|---|---|
| 5470798 | 1008984043 | 20060508 |