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
126262301 12626230 1 I 20160722 20160728 20160805 20160805 EXP FR-JNJFOC-20160725667 JANSSEN 22.00 YR A F Y 0.00000 20160805 PH FR FR

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
126262301 12626230 1 PS STELARA USTEKINUMAB 1 Subcutaneous N 125261 90 MG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126262301 12626230 1 Crohn's disease

Outcome of event

Event ID CASEID OUTC COD
126262301 12626230 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126262301 12626230 Dehydration
126262301 12626230 Diarrhoea
126262301 12626230 Incorrect product storage
126262301 12626230 Malaise
126262301 12626230 Off label use
126262301 12626230 Product use issue

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

no results found

Therapies reported

no results found