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
122693875 12269387 5 F 20160410 20160721 20160414 20160808 EXP CA-JNJFOC-20160410848 JANSSEN 51.09 YR A F Y 70.40000 KG 20160808 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
122693875 12269387 1 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N 0 400 MG LYOPHILIZED POWDER
122693875 12269387 2 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N 0 400 MG LYOPHILIZED POWDER
122693875 12269387 3 PS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N 103772 400 MG LYOPHILIZED POWDER
122693875 12269387 4 C IMURAN AZATHIOPRINE 1 Oral 0 100 MG UNSPECIFIED QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122693875 12269387 1 Colitis ulcerative
122693875 12269387 2 Colitis ulcerative
122693875 12269387 3 Colitis ulcerative

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
122693875 12269387 Frequent bowel movements
122693875 12269387 General physical health deterioration
122693875 12269387 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
122693875 12269387 1 20130913 0
122693875 12269387 2 20160721 0
122693875 12269387 3 20160609 0