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
126127902 12612790 2 F 20160815 20160801 20160819 PER US-AMGEN-USASL2016097871 AMGEN 58.00 YR A F Y 0.00000 20160819 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
126127902 12612790 1 PS ENBREL ETANERCEPT 1 Unknown 50 MG, QWK 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
126127902 12612790 2 SS ENBREL ETANERCEPT 1 Unknown 50 MG, QWK 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
126127902 12612790 3 SS CIMZIA CERTOLIZUMAB PEGOL 1 Unknown UNK 0
126127902 12612790 4 SS CIMZIA CERTOLIZUMAB PEGOL 1 Unknown UNK UNK, Q2WK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126127902 12612790 1 Rheumatoid arthritis
126127902 12612790 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126127902 12612790 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126127902 12612790 Asthenia
126127902 12612790 Dizziness
126127902 12612790 Fatigue
126127902 12612790 Feeling abnormal
126127902 12612790 Headache
126127902 12612790 Lethargy
126127902 12612790 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
126127902 12612790 1 2002 0