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
113393025 11339302 5 F 2015 20160708 20150804 20160719 EXP DE-AMGEN-DEUSP2015078425 AMGEN 65.00 YR E M Y 0.00000 20160718 CN DE DE

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
113393025 11339302 1 PS ENBREL ETANERCEPT 1 Unknown 50 MG, WEEKLY 805 MG Y L16596 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
113393025 11339302 2 SS ENBREL ETANERCEPT 1 Unknown UNK 805 MG Y 103795 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
113393025 11339302 3 SS ENBREL ETANERCEPT 1 Unknown UNK, EVERY 14 DAYS 805 MG Y 103795 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
113393025 11339302 4 C METHOTREXATE (METHOTREXATE SODIUM) METHOTREXATE SODIUM 1 UNK, AS NEEDED 0
113393025 11339302 5 C TILIDINE TILIDINE 1 UNK, AS NEEDED 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113393025 11339302 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
113393025 11339302 OT
113393025 11339302 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
113393025 11339302 Arthritis infective
113393025 11339302 Arthropathy
113393025 11339302 Condition aggravated
113393025 11339302 Off label use
113393025 11339302 Pain in extremity
113393025 11339302 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
113393025 11339302 1 20150326 20150805 0
113393025 11339302 2 2015 0
113393025 11339302 3 20160708 0