Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 82015282 | 8201528 | 2 | F | 20101110 | 20121015 | 20111027 | 20121029 | EXP | FR-AMGEN-FRACT2010007466 | AMGEN | 10.00 | YR | M | Y | 55.80000 | KG | 20121028 | MD | FR | FR |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 82015282 | 8201528 | 1 | PS | etanercept | 1 | SUBCUTANEOUS | 0.8 MG/KG WEEKLY | 38.885 | MG/KG | N | 103795 | .8 | MG/KG | Solution for injection in pre-filled syringe | /wk | ||||
| 82015282 | 8201528 | 2 | SS | etanercept | 1 | SUBCUTANEOUS | 0.8 MG/KG, UNK | 38.885 | MG/KG | N | 103795 | .8 | MG/KG | Solution for injection in pre-filled syringe |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 82015282 | 8201528 | 1 | JUVENILE ARTHRITIS |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 82015282 | 8201528 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 82015282 | 8201528 | Peritonitis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 82015282 | 8201528 | 1 | 20091209 | 20101110 | 0 | |
| 82015282 | 8201528 | 2 | 20101222 | 0 |