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
125221621 12522162 1 I 20160613 20160701 20160701 EXP GB-JNJFOC-20160613909 JANSSEN 0.00 E F Y 0.00000 20160701 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
125221621 12522162 1 PS STELARA USTEKINUMAB 1 Subcutaneous ON WEEK 0 U U UNKNOWN 125261 45 MG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125221621 12522162 1 Psoriatic arthropathy

Outcome of event

Event ID CASEID OUTC COD
125221621 12522162 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125221621 12522162 Cellulitis

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found