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
105892164 10589216 4 F 2014 20160627 20141118 20160704 PER US-AMGEN-USASL2014089088 AMGEN 62.00 YR A F Y 0.00000 20160703 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
105892164 10589216 1 PS ENBREL ETANERCEPT 1 Unknown 50 MG, QWK Y 1045373 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
105892164 10589216 2 SS ENBREL ETANERCEPT 1 Y 103795 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
105892164 10589216 3 SS REMICADE INFLIXIMAB 1 Unknown UNK 0 INFUSION
105892164 10589216 4 C METHOTREXATE. METHOTREXATE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105892164 10589216 1 Psoriatic arthropathy
105892164 10589216 2 Psoriasis
105892164 10589216 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
105892164 10589216 HO
105892164 10589216 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
105892164 10589216 Arthralgia
105892164 10589216 Back pain
105892164 10589216 Breast cancer
105892164 10589216 Condition aggravated
105892164 10589216 Drug ineffective
105892164 10589216 Fatigue
105892164 10589216 Fibromyalgia
105892164 10589216 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
105892164 10589216 1 20140310 0
105892164 10589216 4 201410 0