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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125768801 | 12576880 | 1 | I | 20160712 | 20160720 | 20160720 | EXP | CA-PFIZER INC-2016350830 | PFIZER | 0.00 | F | Y | 0.00000 | 20160720 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125768801 | 12576880 | 1 | SS | ENBREL | ETANERCEPT | 1 | Subcutaneous | UNK | U | 0 | |||||||||
125768801 | 12576880 | 2 | PS | METHOTREXATE. | METHOTREXATE | 1 | Unknown | UNK | U | 11719 | |||||||||
125768801 | 12576880 | 3 | SS | SULFASALAZINE. | SULFASALAZINE | 1 | Unknown | UNK | U | 7073 | |||||||||
125768801 | 12576880 | 4 | SS | FOLIC ACID. | FOLIC ACID | 1 | Unknown | UNK | U | 0 | |||||||||
125768801 | 12576880 | 5 | SS | ACTEMRA | TOCILIZUMAB | 1 | Unknown | UNK | U | 0 | |||||||||
125768801 | 12576880 | 6 | SS | ARAVA | LEFLUNOMIDE | 1 | Unknown | UNK | U | 0 | TABLET | ||||||||
125768801 | 12576880 | 7 | SS | CIMZIA | CERTOLIZUMAB PEGOL | 1 | Subcutaneous | UNK | U | 0 | |||||||||
125768801 | 12576880 | 8 | SS | FOSAMAX | ALENDRONATE SODIUM | 1 | Unknown | UNK | U | 0 | TABLET | ||||||||
125768801 | 12576880 | 9 | SS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | UNK | U | 0 | |||||||||
125768801 | 12576880 | 10 | SS | ORENCIA | ABATACEPT | 1 | Intravenous (not otherwise specified) | UNK | U | 0 | |||||||||
125768801 | 12576880 | 11 | SS | PLAQUENIL | HYDROXYCHLOROQUINE SULFATE | 1 | Unknown | UNK | U | 0 | TABLET | ||||||||
125768801 | 12576880 | 12 | SS | PREDNISONE. | PREDNISONE | 1 | Unknown | UNK | U | 0 | |||||||||
125768801 | 12576880 | 13 | SS | REACTINE | CETIRIZINE HYDROCHLORIDE | 1 | Unknown | UNK | U | 0 | |||||||||
125768801 | 12576880 | 14 | SS | REMICADE | INFLIXIMAB | 1 | Intravenous (not otherwise specified) | UNK | U | 0 | |||||||||
125768801 | 12576880 | 15 | SS | RITUXAN | RITUXIMAB | 1 | Intravenous (not otherwise specified) | UNK | U | 0 | |||||||||
125768801 | 12576880 | 16 | SS | SIMPONI | GOLIMUMAB | 1 | Subcutaneous | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125768801 | 12576880 | 1 | Rheumatoid arthritis |
125768801 | 12576880 | 2 | Rheumatoid arthritis |
125768801 | 12576880 | 3 | Rheumatoid arthritis |
125768801 | 12576880 | 5 | Rheumatoid arthritis |
125768801 | 12576880 | 6 | Rheumatoid arthritis |
125768801 | 12576880 | 7 | Rheumatoid arthritis |
125768801 | 12576880 | 8 | Rheumatoid arthritis |
125768801 | 12576880 | 9 | Rheumatoid arthritis |
125768801 | 12576880 | 10 | Rheumatoid arthritis |
125768801 | 12576880 | 11 | Rheumatoid arthritis |
125768801 | 12576880 | 12 | Rheumatoid arthritis |
125768801 | 12576880 | 14 | Rheumatoid arthritis |
125768801 | 12576880 | 15 | Rheumatoid arthritis |
125768801 | 12576880 | 16 | Rheumatoid arthritis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125768801 | 12576880 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125768801 | 12576880 | Abdominal discomfort | |
125768801 | 12576880 | Alopecia | |
125768801 | 12576880 | Fatigue | |
125768801 | 12576880 | Glossodynia | |
125768801 | 12576880 | Hand deformity | |
125768801 | 12576880 | Pain | |
125768801 | 12576880 | Pemphigus | |
125768801 | 12576880 | Swelling | |
125768801 | 12576880 | Systemic lupus erythematosus | |
125768801 | 12576880 | Wound |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |