The Safety Rates Drug Report

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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
124990912 12499091 2 F 2013 20160920 20160627 20160927 EXP CA-AMGEN-CANSP2016080246 AMGEN 71.00 YR E F Y 0.00000 20160927 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
124990912 12499091 1 PS ENBREL ETANERCEPT 1 Subcutaneous 50 MG, QWEEK U 103795 50 MG UNKNOWN FORMULATION /wk
124990912 12499091 2 SS ARAVA LEFLUNOMIDE 1 Unknown 20 MG, DAILY 0 20 MG QD
124990912 12499091 3 SS PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 Unknown UNK 0
124990912 12499091 4 SS SULFASALAZINE. SULFASALAZINE 1 Oral UNK 0
124990912 12499091 5 SS CIMZIA CERTOLIZUMAB PEGOL 1 Unknown 200 MG, EVERY OTHER WEEK 0 200 MG QOW
124990912 12499091 6 SS HUMIRA ADALIMUMAB 1 Unknown 40 MG, EVERY OTHER WEEK 0 40 MG QOW
124990912 12499091 7 SS ORENCIA ABATACEPT 1 Intravenous (not otherwise specified) 500 MG, EVERY FOUR WEEKS 0 500 MG
124990912 12499091 8 SS METHOTREXATE. METHOTREXATE 1 Oral 25 MG, QWK 0 25 MG /wk
124990912 12499091 9 SS METHOTREXATE. METHOTREXATE 1 Oral 17.5 MG, QWEEK 0 17.5 MG /wk
124990912 12499091 10 C LEUCOVORIN. LEUCOVORIN 1 UNK 0
124990912 12499091 11 C VITAMIN D CHOLECALCIFEROL 1 2000 IU, UNK 0 2000 IU
124990912 12499091 12 C COVERSYL PERINDOPRIL 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124990912 12499091 1 Rheumatoid arthritis
124990912 12499091 2 Product used for unknown indication
124990912 12499091 3 Product used for unknown indication
124990912 12499091 4 Rheumatoid arthritis
124990912 12499091 5 Product used for unknown indication
124990912 12499091 6 Product used for unknown indication
124990912 12499091 7 Product used for unknown indication
124990912 12499091 8 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
124990912 12499091 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124990912 12499091 Affect lability
124990912 12499091 Anxiety
124990912 12499091 Finger deformity
124990912 12499091 Foot operation
124990912 12499091 Headache
124990912 12499091 Hyperhidrosis
124990912 12499091 Joint swelling
124990912 12499091 Nausea
124990912 12499091 Osteoarthritis
124990912 12499091 Palpitations
124990912 12499091 Rheumatoid arthritis
124990912 12499091 Therapeutic response decreased

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
124990912 12499091 1 200503 2013 0
124990912 12499091 5 201311 201404 0
124990912 12499091 6 201303 201309 0
124990912 12499091 7 201405 20160606 0
124990912 12499091 8 200210 0
124990912 12499091 9 201208 0