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
88940122 8894012 2 F 2010 20160901 20121107 20160906 PER US-AMGEN-USASP2011061956 AMGEN 59.00 YR A F Y 0.00000 20160906 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
88940122 8894012 1 PS ENBREL ETANERCEPT 1 Unknown 25 MG, 2 TIMES/WK U 103795 25 MG POWDER AND SOLVENT FOR SOLUTION FOR INJECTION BIW
88940122 8894012 2 SS ENBREL ETANERCEPT 1 U 103795 POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
88940122 8894012 3 SS ENBREL ETANERCEPT 1 U 103795 POWDER AND SOLVENT FOR SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
88940122 8894012 1 Rheumatoid arthritis
88940122 8894012 2 Psoriasis
88940122 8894012 3 Psoriatic arthropathy

Outcome of event

Event ID CASEID OUTC COD
88940122 8894012 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
88940122 8894012 Arthralgia
88940122 8894012 Bone graft
88940122 8894012 Condition aggravated
88940122 8894012 Impaired healing
88940122 8894012 Pain in extremity
88940122 8894012 Psoriasis
88940122 8894012 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
88940122 8894012 1 2010 2012 0