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
99238482 9923848 2 F 20130716 20140127 20140225 20140225 PER US-AMGEN-USASP2013073118 AMGEN 66.00 YR F Y 0.00000 20140225 N 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
99238482 9923848 1 PS Enbrel 1 UNKNOWN 50 MG, WEEKLY 679.245 MG D 1038915 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
99238482 9923848 2 SS Enbrel 1 679.245 MG D 103795 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
99238482 9923848 3 C HUMIRA 1 UNK D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
99238482 9923848 1 Psoriatic arthropathy
99238482 9923848 2 Psoriasis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
99238482 9923848 Arthralgia
99238482 9923848 Contusion
99238482 9923848 Drug ineffective
99238482 9923848 Hypoaesthesia
99238482 9923848 Nail pitting
99238482 9923848 Paraesthesia
99238482 9923848 Skin exfoliation
99238482 9923848 Skin hypertrophy

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
99238482 9923848 1 20130716 0
99238482 9923848 3 20131119 0