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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126126931 | 12612693 | 1 | I | 20151130 | 20160801 | 20160801 | EXP | CA-AMGEN-CANSP2015128883 | AMGEN | 71.00 | YR | E | F | Y | 0.00000 | 20160801 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126126931 | 12612693 | 1 | PS | ENBREL | ETANERCEPT | 1 | Subcutaneous | UNK | U | 103795 | UNKNOWN FORMULATION | ||||||||
| 126126931 | 12612693 | 2 | SS | ACTEMRA | TOCILIZUMAB | 1 | Unknown | UNK | 0 | ||||||||||
| 126126931 | 12612693 | 3 | SS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | UNK | 0 | ||||||||||
| 126126931 | 12612693 | 4 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Subcutaneous | 25 MG, Q WEEKLY | 0 | 25 | MG | /wk | |||||||
| 126126931 | 12612693 | 5 | SS | SULFASALAZINE. | SULFASALAZINE | 1 | Unknown | 500 MG, UNK | 0 | 500 | MG | ||||||||
| 126126931 | 12612693 | 6 | SS | HYDROXYCHLOROQUINE | HYDROXYCHLOROQUINE | 1 | Unknown | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126126931 | 12612693 | 1 | Rheumatoid arthritis |
| 126126931 | 12612693 | 2 | Rheumatoid arthritis |
| 126126931 | 12612693 | 3 | Rheumatoid arthritis |
| 126126931 | 12612693 | 4 | Rheumatoid arthritis |
| 126126931 | 12612693 | 5 | Rheumatoid arthritis |
| 126126931 | 12612693 | 6 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126126931 | 12612693 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126126931 | 12612693 | Drug ineffective | |
| 126126931 | 12612693 | Drug intolerance | |
| 126126931 | 12612693 | Dyspepsia | |
| 126126931 | 12612693 | Nausea | |
| 126126931 | 12612693 | Thrombosis | |
| 126126931 | 12612693 | Treatment failure |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |