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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
116290023 | 11629002 | 3 | F | 20160712 | 20151014 | 20160715 | EXP | CA-AMGEN-CANSP2015106456 | AMGEN | 23.00 | YR | A | F | Y | 0.00000 | 20160715 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
116290023 | 11629002 | 1 | PS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | U | 103795 | UNKNOWN FORMULATION | ||||||||
116290023 | 11629002 | 2 | SS | ENBREL | ETANERCEPT | 1 | U | 103795 | UNKNOWN FORMULATION | ||||||||||
116290023 | 11629002 | 3 | SS | METHOTREXATE SODIUM. | METHOTREXATE SODIUM | 1 | Unknown | UNK | 0 | ||||||||||
116290023 | 11629002 | 4 | SS | REMICADE | INFLIXIMAB | 1 | Unknown | UNK | 0 | ||||||||||
116290023 | 11629002 | 5 | SS | RITUXAN | RITUXIMAB | 1 | Unknown | UNK | 0 | ||||||||||
116290023 | 11629002 | 6 | C | PREDNISONE. | PREDNISONE | 1 | UNK | 0 | |||||||||||
116290023 | 11629002 | 7 | C | ARAVA | LEFLUNOMIDE | 1 | UNK | 0 | |||||||||||
116290023 | 11629002 | 8 | C | ACTEMRA | TOCILIZUMAB | 1 | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
116290023 | 11629002 | 1 | Rheumatoid arthritis |
116290023 | 11629002 | 2 | Juvenile idiopathic arthritis |
116290023 | 11629002 | 3 | Rheumatoid arthritis |
116290023 | 11629002 | 4 | Rheumatoid arthritis |
116290023 | 11629002 | 5 | Rheumatoid arthritis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
116290023 | 11629002 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
116290023 | 11629002 | Activities of daily living impaired | |
116290023 | 11629002 | Drug dose omission | |
116290023 | 11629002 | Drug effect decreased | |
116290023 | 11629002 | Drug ineffective | |
116290023 | 11629002 | Rheumatoid arthritis |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |