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
126079454 12607945 4 F 2016 20160923 20160729 20160929 EXP GB-JNJFOC-20160715284 JANSSEN 61.56 YR A F Y 0.00000 20160929 CN GB GB

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
126079454 12607945 1 PS STELARA USTEKINUMAB 1 Subcutaneous 45 MG/0.5 ML PRE-FILLED SYRINGE Y N FHS3YMU 125261 45 MG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126079454 12607945 1 Psoriatic arthropathy

Outcome of event

Event ID CASEID OUTC COD
126079454 12607945 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126079454 12607945 Cold sweat
126079454 12607945 Dizziness
126079454 12607945 Dyspnoea
126079454 12607945 Fatigue
126079454 12607945 Feeling hot
126079454 12607945 Heart rate increased
126079454 12607945 Hypersensitivity
126079454 12607945 Hypertension
126079454 12607945 Malaise
126079454 12607945 Pallor
126079454 12607945 Paraesthesia
126079454 12607945 Sensory disturbance

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
126079454 12607945 1 20160712 0