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
112265232 11226523 2 F 2015 20160719 20150629 20160727 EXP BR-AMGEN-BRASP2015032666 AMGEN 18.00 YR A F Y 47.00000 KG 20160726 CN BR BR

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
112265232 11226523 1 PS ENBREL ETANERCEPT 1 Subcutaneous 50 MG, ONCE WEEKLY 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
112265232 11226523 2 C PREDNISONE. PREDNISONE 1 UNK 0
112265232 11226523 3 C OMEGA 3 COMPLETE 2 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112265232 11226523 1 Juvenile idiopathic arthritis

Outcome of event

Event ID CASEID OUTC COD
112265232 11226523 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
112265232 11226523 Injection site erythema
112265232 11226523 Joint swelling
112265232 11226523 Pruritus
112265232 11226523 Wrong technique in product usage process

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
112265232 11226523 1 201302 0