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
119817053 11981705 3 F 20160621 20160131 20160705 PER US-AMGEN-USASL2016009402 AMGEN 30.00 YR A F Y 0.00000 20160704 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
119817053 11981705 1 PS ENBREL ETANERCEPT 1 Unknown 50 MG, WEEKLY U 1062648 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
119817053 11981705 2 SS ENBREL ETANERCEPT 1 Unknown UNK UNK, UNK U 1057436 103795 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
119817053 11981705 3 SS ENBREL ETANERCEPT 1 Unknown UNK U 1064412 103795 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
119817053 11981705 4 SS CELEBREX CELECOXIB 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119817053 11981705 1 Psoriatic arthropathy
119817053 11981705 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
119817053 11981705 Arthralgia
119817053 11981705 Back pain
119817053 11981705 Condition aggravated
119817053 11981705 Drug ineffective
119817053 11981705 Dyspepsia
119817053 11981705 Gait disturbance
119817053 11981705 Musculoskeletal chest pain
119817053 11981705 Musculoskeletal stiffness
119817053 11981705 Pain
119817053 11981705 Pain in extremity
119817053 11981705 Sacroiliitis

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
119817053 11981705 1 20151111 0
119817053 11981705 3 20160609 0