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
100640756 10064075 6 F 2012 20140923 20140408 20140930 EXP US-AMGEN-USASP2014024214 AMGEN 47.00 YR A M Y 90.70000 KG 20140930 N CN 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
100640756 10064075 1 PS ENBREL ETANERCEPT 1 SUBCUTANEOUS 50 MG, QWK D 1033748 103795 50 MG /wk
100640756 10064075 2 C PLAQUENIL HYDROXYCHLOROQUINE SULFATE 1 400 MG, A DAY D 0 400 MG QD
100640756 10064075 3 C PREDNISONE. PREDNISONE 1 VARIABLE DOSE D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100640756 10064075 1 Rheumatoid arthritis
100640756 10064075 3 Ear infection

Outcome of event

Event ID CASEID OUTC COD
100640756 10064075 OT
100640756 10064075 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
100640756 10064075 Arthralgia
100640756 10064075 Arthropathy
100640756 10064075 Blindness
100640756 10064075 Blood pressure increased
100640756 10064075 Drug effect incomplete
100640756 10064075 Ear infection
100640756 10064075 General symptom
100640756 10064075 Headache
100640756 10064075 Hypoaesthesia
100640756 10064075 Joint crepitation
100640756 10064075 Joint lock
100640756 10064075 Joint stiffness
100640756 10064075 Joint swelling
100640756 10064075 Limb discomfort
100640756 10064075 Local swelling
100640756 10064075 Mass
100640756 10064075 Mobility decreased
100640756 10064075 Musculoskeletal discomfort
100640756 10064075 Musculoskeletal stiffness
100640756 10064075 Pain
100640756 10064075 Pain in extremity
100640756 10064075 Pericarditis
100640756 10064075 Sensory disturbance
100640756 10064075 Sleep disorder
100640756 10064075 Temporal arteritis

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
100640756 10064075 1 201205 20140430 0