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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 106634863 | 10663486 | 3 | F | 20160825 | 20141219 | 20160902 | EXP | SE-AMGEN-SWESP2014098097 | AMGEN | 0.00 | E | M | Y | 0.00000 | 20160902 | CN | SE | SE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 106634863 | 10663486 | 1 | PS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | 103795 | UNKNOWN FORMULATION | |||||||||
| 106634863 | 10663486 | 2 | I | METHOTREXATE ORION | METHOTREXATE | 1 | Unknown | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 106634863 | 10663486 | 1 | Rheumatoid arthritis |
| 106634863 | 10663486 | 2 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 106634863 | 10663486 | LT |
| 106634863 | 10663486 | OT |
| 106634863 | 10663486 | HO |
| 106634863 | 10663486 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 106634863 | 10663486 | Bacterial infection | |
| 106634863 | 10663486 | Coma | |
| 106634863 | 10663486 | Drug dose omission | |
| 106634863 | 10663486 | Drug interaction | |
| 106634863 | 10663486 | Musculoskeletal disorder |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |