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
106778792 10677879 2 F 201402 20160719 20141229 20160724 EXP BR-AMGEN-BRASP2014100458 AMGEN 44.00 YR A F Y 59.00000 KG 20160724 CN BR BR

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
106778792 10677879 1 PS ENBREL ETANERCEPT 1 Subcutaneous 50 MG, 1X/WEEK 103795 50 MG SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE /wk
106778792 10677879 2 C ARAVA LEFLUNOMIDE 1 1 TABLET (20 MG), 1X/DAY 0 20 MG TABLET QD
106778792 10677879 3 C RIVOTRIL CLONAZEPAM 1 1 TABLET (3 MG), 2X/DAY 0 3 MG TABLET BID
106778792 10677879 4 C PREDNISONE. PREDNISONE 1 5 MG, UNK 0 5 MG
106778792 10677879 5 C ANTI INFLAMMATORY 2 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106778792 10677879 1 Psoriatic arthropathy

Outcome of event

Event ID CASEID OUTC COD
106778792 10677879 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
106778792 10677879 Depressed mood
106778792 10677879 Dyspnoea
106778792 10677879 Fatigue
106778792 10677879 Fear
106778792 10677879 Irritability
106778792 10677879 Malaise
106778792 10677879 Pneumonia
106778792 10677879 Sinusitis
106778792 10677879 Viral infection

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
106778792 10677879 1 201306 0
106778792 10677879 3 201409 0