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
126007511 12600751 1 I 20160711 20160720 20160727 20160727 EXP CA-AMGEN-CANSP2016095790 AMGEN 68.00 YR E F Y 0.00000 20160727 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
126007511 12600751 1 PS ENBREL ETANERCEPT 1 Unknown 25 MG, UNK U 103795 25 MG UNKNOWN FORMULATION
126007511 12600751 2 SS METHOTREXATE. METHOTREXATE 1 Unknown 25 MG, UNK 0 25 MG
126007511 12600751 3 SS ORENCIA ABATACEPT 1 Unknown 500 MG, UNK 0 500 MG
126007511 12600751 4 SS ACTEMRA TOCILIZUMAB 1 Unknown UNK 0
126007511 12600751 5 SS CIMZIA CERTOLIZUMAB PEGOL 1 Unknown UNK 0
126007511 12600751 6 SS SIMPONI GOLIMUMAB 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126007511 12600751 1 Rheumatoid arthritis
126007511 12600751 2 Rheumatoid arthritis
126007511 12600751 3 Product used for unknown indication
126007511 12600751 4 Product used for unknown indication
126007511 12600751 5 Product used for unknown indication
126007511 12600751 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126007511 12600751 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126007511 12600751 Drug ineffective
126007511 12600751 Drug intolerance
126007511 12600751 Joint swelling
126007511 12600751 Rheumatoid arthritis

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
126007511 12600751 1 201102 201105 0
126007511 12600751 2 200912 201312 0
126007511 12600751 3 201311 201404 0