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
122351194 12235119 4 F 20151105 20160701 20160404 20160711 EXP TW-JNJFOC-20160321564 JANSSEN 56.28 YR A M Y 96.00000 KG 20160711 OT TW TW

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
122351194 12235119 1 SS STELARA USTEKINUMAB 1 Subcutaneous Y N 0 45 MG SOLUTION FOR INJECTION
122351194 12235119 2 PS STELARA USTEKINUMAB 1 Subcutaneous Y N 125261 45 MG SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122351194 12235119 1 Psoriasis
122351194 12235119 2 Psoriasis

Outcome of event

Event ID CASEID OUTC COD
122351194 12235119 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122351194 12235119 Mycobacterium fortuitum infection
122351194 12235119 Off label use
122351194 12235119 Product use issue

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
122351194 12235119 1 20151105 0
122351194 12235119 2 20151201 0