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
108881684 10888168 4 F 20150814 20160714 20150304 20160728 EXP AR-AMGEN-ARGSP2015019001 AMGEN 53.00 YR A F Y 0.00000 20160728 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
108881684 10888168 1 PS ENBREL ETANERCEPT 1 Unknown 50 MG, WEEKLY M24512 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
108881684 10888168 2 SS ENBREL ETANERCEPT 1 Unknown 50 MG, WEEKLY 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
108881684 10888168 3 SS ENBREL ETANERCEPT 1 Unknown 50 MG, WEEKLY L39976 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
108881684 10888168 1 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
108881684 10888168 HO
108881684 10888168 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
108881684 10888168 Bone disorder
108881684 10888168 Condition aggravated
108881684 10888168 Gastric ulcer
108881684 10888168 Intervertebral disc protrusion
108881684 10888168 Nerve compression
108881684 10888168 Osteoporosis
108881684 10888168 Rheumatoid arthritis
108881684 10888168 Sciatic nerve neuropathy

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
108881684 10888168 1 20090715 201412 0