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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6451694 | 7185381 | I | 6451694-0 | 20081118 | 20081119 | 20091123 | PER | US-AMGEN-KDL319895 | AMGENSAFETY | 51 | F | Y | 20091123 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6451694 | 1012628198 | PS | ENBREL | 1 | SUBCUTANEOUS | P109307 | |||||
| 6451694 | 1012628199 | SS | ENBREL | 1 | P109307 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6451694 | 1012628198 | PSORIASIS |
| 6451694 | 1012628199 | PSORIATIC ARTHROPATHY |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 6451694 | INJECTION SITE ERYTHEMA |
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 |
|---|---|---|---|---|---|
| 6451694 | 1012628198 | 20081105 |