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
127208961 12720896 1 I 2016 20160830 20160907 20160907 EXP SE-JNJFOC-20160901799 JANSSEN 69.00 YR E F Y 0.00000 20160907 CN SE SE

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
127208961 12720896 1 SS STELARA USTEKINUMAB 1 Subcutaneous N 0 45 MG SOLUTION FOR INJECTION
127208961 12720896 2 PS STELARA USTEKINUMAB 1 Subcutaneous N 125261 45 MG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127208961 12720896 1 Psoriatic arthropathy
127208961 12720896 2 Psoriatic arthropathy

Outcome of event

Event ID CASEID OUTC COD
127208961 12720896 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127208961 12720896 Atrial fibrillation
127208961 12720896 Inappropriate schedule of drug administration
127208961 12720896 Off label use

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
127208961 12720896 1 2016 0