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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117453813 | 11745381 | 3 | F | 20160714 | 20151117 | 20160720 | EXP | CA-AMGEN-CANSP2015120647 | AMGEN | 49.00 | YR | A | F | Y | 0.00000 | 20160719 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 117453813 | 11745381 | 1 | PS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | U | 103795 | UNKNOWN FORMULATION | ||||||||
| 117453813 | 11745381 | 2 | SS | METHOTREXATE. | METHOTREXATE | 1 | Unknown | UNK | 0 | ||||||||||
| 117453813 | 11745381 | 3 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | Unknown | UNK | 0 | ||||||||||
| 117453813 | 11745381 | 4 | SS | ARAVA | LEFLUNOMIDE | 1 | Unknown | UNK | 0 | ||||||||||
| 117453813 | 11745381 | 5 | SS | GOLD | GOLD | 1 | Unknown | UNK | 0 | ||||||||||
| 117453813 | 11745381 | 6 | SS | HUMIRA | ADALIMUMAB | 1 | Unknown | UNK | 0 | ||||||||||
| 117453813 | 11745381 | 7 | SS | ORENCIA | ABATACEPT | 1 | Unknown | UNK | 0 | ||||||||||
| 117453813 | 11745381 | 8 | SS | ACTEMRA | TOCILIZUMAB | 1 | Unknown | UNK | 0 | ||||||||||
| 117453813 | 11745381 | 9 | SS | REMICADE | INFLIXIMAB | 1 | Unknown | UNK | 0 | ||||||||||
| 117453813 | 11745381 | 10 | SS | RITUXAN | RITUXIMAB | 1 | Unknown | UNK | 0 | ||||||||||
| 117453813 | 11745381 | 11 | SS | ROCURONIUM | ROCURONIUM BROMIDE | 1 | Unknown | UNK | 0 | ||||||||||
| 117453813 | 11745381 | 12 | SS | CODEINE | CODEINE | 1 | Unknown | UNK | 0 | ||||||||||
| 117453813 | 11745381 | 13 | C | PREDNISONE. | PREDNISONE | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 117453813 | 11745381 | 1 | Rheumatoid arthritis |
| 117453813 | 11745381 | 2 | Rheumatoid arthritis |
| 117453813 | 11745381 | 3 | Rheumatoid arthritis |
| 117453813 | 11745381 | 4 | Rheumatoid arthritis |
| 117453813 | 11745381 | 5 | Rheumatoid arthritis |
| 117453813 | 11745381 | 6 | Rheumatoid arthritis |
| 117453813 | 11745381 | 7 | Rheumatoid arthritis |
| 117453813 | 11745381 | 8 | Rheumatoid arthritis |
| 117453813 | 11745381 | 9 | Rheumatoid arthritis |
| 117453813 | 11745381 | 10 | Rheumatoid arthritis |
| 117453813 | 11745381 | 11 | Product used for unknown indication |
| 117453813 | 11745381 | 12 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 117453813 | 11745381 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 117453813 | 11745381 | Anaphylactic reaction | |
| 117453813 | 11745381 | Arthropathy | |
| 117453813 | 11745381 | Condition aggravated | |
| 117453813 | 11745381 | Drug hypersensitivity | |
| 117453813 | 11745381 | Finger deformity | |
| 117453813 | 11745381 | Limb operation | |
| 117453813 | 11745381 | Peripheral swelling | |
| 117453813 | 11745381 | Rash | |
| 117453813 | 11745381 | Tenosynovitis | |
| 117453813 | 11745381 | Treatment failure | |
| 117453813 | 11745381 | Urticaria | |
| 117453813 | 11745381 | Wrist surgery |
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 |
|---|---|---|---|---|---|---|
| 117453813 | 11745381 | 10 | 20150808 | 0 |