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
113111805 11311180 5 F 201507 20160714 20150727 20160722 PER US-AMGEN-USASP2015073138 AMGEN 63.00 YR A F Y 0.00000 20160722 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
113111805 11311180 1 PS ENBREL ETANERCEPT 1 Subcutaneous 50 MG, ONCE A WEEK U 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
113111805 11311180 2 SS ENBREL ETANERCEPT 1 Unknown 25 MG, ONCE A WEEK U 103795 25 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113111805 11311180 1 Ankylosing spondylitis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
113111805 11311180 Asthenia
113111805 11311180 Injection site bruising
113111805 11311180 Injection site discolouration
113111805 11311180 Injection site erythema
113111805 11311180 Injection site pain
113111805 11311180 Injection site reaction
113111805 11311180 Injection site swelling
113111805 11311180 Rash
113111805 11311180 Tooth disorder

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
113111805 11311180 1 20150615 0