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
122537232 12253723 2 F 20160328 20160728 20160411 20160805 EXP CA-JNJFOC-20160408329 JANSSEN 23.52 YR A F Y 76.00000 KG 20160805 OT CA CA

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
122537232 12253723 1 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N 0 700 MG LYOPHILIZED POWDER
122537232 12253723 2 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N 0 700 MG LYOPHILIZED POWDER
122537232 12253723 3 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N 0 700 MG LYOPHILIZED POWDER
122537232 12253723 4 PS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N 103772 700 MG LYOPHILIZED POWDER

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122537232 12253723 1 Colitis ulcerative
122537232 12253723 2 Colitis ulcerative
122537232 12253723 3 Colitis ulcerative
122537232 12253723 4 Colitis ulcerative

Outcome of event

Event ID CASEID OUTC COD
122537232 12253723 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122537232 12253723 General physical health deterioration
122537232 12253723 Haematochezia

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
122537232 12253723 1 20160728 0
122537232 12253723 2 20160406 0
122537232 12253723 3 20130301 0
122537232 12253723 4 2014 0