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
106900206 10690020 6 F 2014 20160809 20150105 20160812 PER US-AMGEN INC.-USASP2014102549 AMGEN 64.00 YR A M Y 0.00000 20160812 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
106900206 10690020 1 PS ENBREL ETANERCEPT 1 Unknown 50 MG, QWK Y 1050569 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
106900206 10690020 2 SS ENBREL ETANERCEPT 1 Unknown UNK Y 1065293 103795 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
106900206 10690020 3 C CYMBALTA DULOXETINE HYDROCHLORIDE 1 UNK 0
106900206 10690020 4 C METHOTREXATE. METHOTREXATE 1 UNK 0
106900206 10690020 5 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106900206 10690020 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
106900206 10690020 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
106900206 10690020 Device failure
106900206 10690020 Injection site pain
106900206 10690020 Knee arthroplasty
106900206 10690020 Pain
106900206 10690020 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
106900206 10690020 1 20140830 0