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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125709781 | 12570978 | 1 | I | 2007 | 20151106 | 20160719 | 20160719 | EXP | CA-AMGEN-CANSP2015119458 | AMGEN | 41.00 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125709781 | 12570978 | 1 | PS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | U | 103795 | SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE | ||||||||
| 125709781 | 12570978 | 2 | SS | METHOTREXATE. | METHOTREXATE | 1 | Unknown | 25 MG, UNK | 0 | 25 | MG | ||||||||
| 125709781 | 12570978 | 3 | SS | ACTEMRA | TOCILIZUMAB | 1 | Unknown | UNK | 0 | ||||||||||
| 125709781 | 12570978 | 4 | SS | HYDROXYCHLOROQUINE | HYDROXYCHLOROQUINE | 1 | Unknown | 200 MG/DAY | 0 | 200 | MG | QD | |||||||
| 125709781 | 12570978 | 5 | SS | SULFASALAZINE. | SULFASALAZINE | 1 | Unknown | 1500 MG, UNK | 0 | 1500 | MG | ||||||||
| 125709781 | 12570978 | 6 | SS | REMICADE | INFLIXIMAB | 1 | Unknown | UNK | 0 | ||||||||||
| 125709781 | 12570978 | 7 | SS | ORENCIA | ABATACEPT | 1 | Unknown | UNK | 0 | ||||||||||
| 125709781 | 12570978 | 8 | SS | ARAVA | LEFLUNOMIDE | 1 | Unknown | 10 MG, QD | 0 | 10 | MG | TABLET | QD | ||||||
| 125709781 | 12570978 | 9 | C | KINERET | ANAKINRA | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125709781 | 12570978 | 1 | Rheumatoid arthritis |
| 125709781 | 12570978 | 2 | Rheumatoid arthritis |
| 125709781 | 12570978 | 3 | Rheumatoid arthritis |
| 125709781 | 12570978 | 4 | Rheumatoid arthritis |
| 125709781 | 12570978 | 5 | Rheumatoid arthritis |
| 125709781 | 12570978 | 6 | Rheumatoid arthritis |
| 125709781 | 12570978 | 7 | Rheumatoid arthritis |
| 125709781 | 12570978 | 8 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125709781 | 12570978 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125709781 | 12570978 | C-reactive protein abnormal | |
| 125709781 | 12570978 | Drug hypersensitivity | |
| 125709781 | 12570978 | Drug ineffective | |
| 125709781 | 12570978 | Drug intolerance | |
| 125709781 | 12570978 | Hepatitis | |
| 125709781 | 12570978 | Hypersensitivity | |
| 125709781 | 12570978 | Red blood cell sedimentation rate abnormal | |
| 125709781 | 12570978 | Rheumatoid factor positive | |
| 125709781 | 12570978 | Synovitis | |
| 125709781 | 12570978 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 125709781 | 12570978 | 2 | 2007 | 2008 | 0 |