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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126838351 | 12683835 | 1 | I | 20160818 | 20160825 | 20160825 | EXP | CA-AMGEN-CANSP2016109088 | AMGEN | 60.00 | YR | A | F | Y | 0.00000 | 20160825 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126838351 | 12683835 | 1 | PS | ENBREL | ETANERCEPT | 1 | Unknown | UNK | U | 103795 | UNKNOWN FORMULATION | ||||||||
126838351 | 12683835 | 2 | SS | ACTEMRA | TOCILIZUMAB | 1 | Unknown | UNK | 0 | ||||||||||
126838351 | 12683835 | 3 | SS | CIMZIA | CERTOLIZUMAB PEGOL | 1 | Unknown | UNK | 0 | ||||||||||
126838351 | 12683835 | 4 | SS | HUMIRA | ADALIMUMAB | 1 | Unknown | UNK | 0 | ||||||||||
126838351 | 12683835 | 5 | SS | HYDROXYCHLOROQUINE | HYDROXYCHLOROQUINE | 1 | Unknown | UNK | 0 | ||||||||||
126838351 | 12683835 | 6 | SS | METHOTREXATE. | METHOTREXATE | 1 | Oral | UNK | 0 | ||||||||||
126838351 | 12683835 | 7 | SS | ORENCIA | ABATACEPT | 1 | Unknown | UNK | 0 | ||||||||||
126838351 | 12683835 | 8 | SS | REMICADE | INFLIXIMAB | 1 | Unknown | UNK | 0 | ||||||||||
126838351 | 12683835 | 9 | SS | RITUXAN | RITUXIMAB | 1 | Intravenous (not otherwise specified) | UNK | 0 | ||||||||||
126838351 | 12683835 | 10 | SS | SIMPONI | GOLIMUMAB | 1 | Unknown | UNK | 0 | ||||||||||
126838351 | 12683835 | 11 | SS | SULFASALAZINE. | SULFASALAZINE | 1 | Unknown | UNK | 0 | ||||||||||
126838351 | 12683835 | 12 | SS | XELJANZ | TOFACITINIB CITRATE | 1 | Unknown | 5.0 MG, UNK | 0 | 5 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126838351 | 12683835 | 1 | Rheumatoid arthritis |
126838351 | 12683835 | 2 | Rheumatoid arthritis |
126838351 | 12683835 | 3 | Rheumatoid arthritis |
126838351 | 12683835 | 4 | Rheumatoid arthritis |
126838351 | 12683835 | 5 | Product used for unknown indication |
126838351 | 12683835 | 6 | Rheumatoid arthritis |
126838351 | 12683835 | 7 | Rheumatoid arthritis |
126838351 | 12683835 | 8 | Rheumatoid arthritis |
126838351 | 12683835 | 9 | Product used for unknown indication |
126838351 | 12683835 | 10 | Rheumatoid arthritis |
126838351 | 12683835 | 11 | Rheumatoid arthritis |
126838351 | 12683835 | 12 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126838351 | 12683835 | DS |
126838351 | 12683835 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126838351 | 12683835 | Abdominal discomfort | |
126838351 | 12683835 | Activities of daily living impaired | |
126838351 | 12683835 | Coeliac disease | |
126838351 | 12683835 | Drug ineffective | |
126838351 | 12683835 | Grip strength decreased | |
126838351 | 12683835 | Headache | |
126838351 | 12683835 | Injection site reaction | |
126838351 | 12683835 | Nail disorder | |
126838351 | 12683835 | Onychomadesis | |
126838351 | 12683835 | Onychomycosis |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |