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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123269702 | 12326970 | 2 | F | 20160818 | 20160503 | 20160826 | EXP | CA-AMGEN-CANSP2016054833 | AMGEN | 53.00 | YR | A | M | Y | 0.00000 | 20160826 | OT | CA | CA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123269702 | 12326970 | 1 | PS | ENBREL | ETANERCEPT | 1 | Subcutaneous | UNK | U | 103795 | UNKNOWN FORMULATION | ||||||||
| 123269702 | 12326970 | 2 | SS | ACTEMRA | TOCILIZUMAB | 1 | Unknown | UNK | 0 | ||||||||||
| 123269702 | 12326970 | 3 | SS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | 40 MG, Q2WK | 0 | 40 | MG | QOW | |||||||
| 123269702 | 12326970 | 4 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | Oral | 400 MG, QD | 0 | 400 | MG | TABLET | QD | ||||||
| 123269702 | 12326970 | 5 | SS | REMICADE | INFLIXIMAB | 1 | Intravenous (not otherwise specified) | UNK | 0 | ||||||||||
| 123269702 | 12326970 | 6 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | Unknown | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123269702 | 12326970 | 1 | Rheumatoid arthritis |
| 123269702 | 12326970 | 2 | Product used for unknown indication |
| 123269702 | 12326970 | 3 | Rheumatoid arthritis |
| 123269702 | 12326970 | 4 | Rheumatoid arthritis |
| 123269702 | 12326970 | 5 | Product used for unknown indication |
| 123269702 | 12326970 | 6 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123269702 | 12326970 | DS |
| 123269702 | 12326970 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123269702 | 12326970 | Drug ineffective | |
| 123269702 | 12326970 | Dyspnoea | |
| 123269702 | 12326970 | Joint lock | |
| 123269702 | 12326970 | Mass | |
| 123269702 | 12326970 | Pain | |
| 123269702 | 12326970 | Peripheral swelling | |
| 123269702 | 12326970 | Physical disability |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |