The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
127015711 12701571 1 I 20160818 20160831 20160831 EXP CA-ORION CORPORATION ORION PHARMA-TREX2016-1493 ORION 0.00 F Y 0.00000 20160831 MD 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
127015711 12701571 1 PS METHOTREXATE (TRADE NAME UNKNOWN) METHOTREXATE 1 Unknown U 0 20 MG /wk
127015711 12701571 2 SS ENBREL ETANERCEPT 1 Subcutaneous U 0 50 MG
127015711 12701571 3 SS ACTEMRA TOCILIZUMAB 1 Subcutaneous U 0
127015711 12701571 4 SS ACTEMRA TOCILIZUMAB 1 Intravenous (not otherwise specified) U 0
127015711 12701571 5 SS HUMIRA ADALIMUMAB 1 Subcutaneous U 0 40 MG BIW
127015711 12701571 6 SS LEFLUNOMIDE. LEFLUNOMIDE 1 Unknown U 0 20 MG TABLET
127015711 12701571 7 SS ORENCIA ABATACEPT 1 Intravenous (not otherwise specified) U 0 750 MG QID
127015711 12701571 8 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) U 0 5 MG/KG
127015711 12701571 9 C XELJANZ TOFACITINIB CITRATE 1 Unknown 0
127015711 12701571 10 C CIMZIA CERTOLIZUMAB PEGOL 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127015711 12701571 1 Rheumatoid arthritis
127015711 12701571 2 Rheumatoid arthritis
127015711 12701571 7 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
127015711 12701571 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127015711 12701571 Arthropathy
127015711 12701571 Drug ineffective
127015711 12701571 Gait disturbance

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found