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
117411552 11741155 2 F 20160907 20151116 20160912 EXP CA-ROCHE-1659443 ROCHE 0.00 M Y 0.00000 20160912 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
117411552 11741155 1 PS ACTEMRA TOCILIZUMAB 1 Unknown U NOT REPORTED 125276
117411552 11741155 2 SS ENBREL ETANERCEPT 1 Subcutaneous U 0
117411552 11741155 3 SS HUMIRA ADALIMUMAB 1 Subcutaneous U 0
117411552 11741155 4 SS ORENCIA ABATACEPT 1 Intravenous (not otherwise specified) U 0
117411552 11741155 5 SS SIMPONI GOLIMUMAB 1 Subcutaneous U 0
117411552 11741155 6 SS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous U 0
117411552 11741155 7 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) U 0
117411552 11741155 8 SS METHOTREXATE. METHOTREXATE 1 Unknown U 0 20 MG /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117411552 11741155 1 Rheumatoid arthritis
117411552 11741155 2 Rheumatoid arthritis
117411552 11741155 3 Rheumatoid arthritis
117411552 11741155 4 Rheumatoid arthritis
117411552 11741155 5 Rheumatoid arthritis
117411552 11741155 6 Rheumatoid arthritis
117411552 11741155 7 Rheumatoid arthritis
117411552 11741155 8 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
117411552 11741155 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117411552 11741155 Drug hypersensitivity
117411552 11741155 Drug ineffective
117411552 11741155 Rheumatoid arthritis

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

no results found

Therapies reported

no results found