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
127113571 12711357 1 I 2015 20160826 20160902 20160902 PER US-AMGEN-USASL2016113792 AMGEN 75.00 YR E F Y 0.00000 20160902 MD US US

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
127113571 12711357 1 PS ENBREL ETANERCEPT 1 Unknown 50 MG, QWK TUESDAY U 1065724 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
127113571 12711357 2 SS ENBREL ETANERCEPT 1 Unknown UNK U 103795 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
127113571 12711357 3 SS CIMZIA CERTOLIZUMAB PEGOL 1 Unknown UNK 0
127113571 12711357 4 SS ACTEMRA TOCILIZUMAB 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127113571 12711357 1 Rheumatoid arthritis
127113571 12711357 3 Product used for unknown indication
127113571 12711357 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127113571 12711357 Drug dose omission
127113571 12711357 Drug effect incomplete
127113571 12711357 Drug ineffective
127113571 12711357 Pain

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
127113571 12711357 1 2015 0