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
106895212 10689521 2 F 201412 20160817 20150105 20160825 PER US-AMGEN INC.-USASP2014102502 AMGEN 68.00 YR E F Y 0.00000 20160824 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
106895212 10689521 1 PS ENBREL ETANERCEPT 1 Unknown 50 MG, QWK 1052264 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
106895212 10689521 2 SS ENBREL ETANERCEPT 1 Unknown UNK 1063617 103795 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
106895212 10689521 3 C ASPIRIN. ASPIRIN 1 UNK UNK, QD 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106895212 10689521 1 Psoriatic arthropathy
106895212 10689521 2 Psoriasis

Outcome of event

Event ID CASEID OUTC COD
106895212 10689521 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
106895212 10689521 Feeling abnormal
106895212 10689521 Fibromyalgia
106895212 10689521 Injection site erythema
106895212 10689521 Injection site haemorrhage
106895212 10689521 Injection site hypertrophy
106895212 10689521 Injection site inflammation
106895212 10689521 Injection site mass
106895212 10689521 Injection site pain
106895212 10689521 Injection site rash
106895212 10689521 Injection site reaction
106895212 10689521 Injection site swelling
106895212 10689521 Injection site warmth
106895212 10689521 Psoriasis

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
106895212 10689521 1 20141210 0