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
82269864 8226986 4 F 2014 20160906 20111103 20160923 PER US-AMGEN-USASP2011037869 AMGEN 47.00 YR A F Y 0.00000 20160922 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
82269864 8226986 1 PS ENBREL ETANERCEPT 1 Unknown 50 MG, QWK N 1025265 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
82269864 8226986 2 SS ARAVA LEFLUNOMIDE 1 Unknown UNK 0
82269864 8226986 3 SS SULFASALAZINE. SULFASALAZINE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
82269864 8226986 1 Rheumatoid arthritis
82269864 8226986 2 Product used for unknown indication
82269864 8226986 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
82269864 8226986 Adverse event
82269864 8226986 Alopecia
82269864 8226986 Injection site pain
82269864 8226986 Pain
82269864 8226986 Stress

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
82269864 8226986 1 20110717 0