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
108648962 10864896 2 F 201412 20160826 20150224 20160910 EXP AR-AMGEN-ARGSP2015016897 AMGEN 51.00 YR A F Y 0.00000 20160909 CN AR AR

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
108648962 10864896 1 PS ENBREL ETANERCEPT 1 Unknown 50 MG, QWK J23953 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
108648962 10864896 2 SS ENBREL ETANERCEPT 1 Unknown 50 MG, QWK M61907 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
108648962 10864896 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
108648962 10864896 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
108648962 10864896 Abdominal pain upper
108648962 10864896 Agitation
108648962 10864896 Arthropathy
108648962 10864896 Bronchospasm
108648962 10864896 Drug ineffective
108648962 10864896 Dyspnoea
108648962 10864896 Haemorrhage
108648962 10864896 Musculoskeletal disorder
108648962 10864896 Pain
108648962 10864896 Spinal disorder

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
108648962 10864896 1 20100715 201605 0
108648962 10864896 2 20160823 0