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
123097544 12309754 4 F 20110729 20160622 20160427 20160701 EXP CA-JNJFOC-20151126258 JANSSEN 13.62 YR C M Y 66.00000 KG 20160701 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
123097544 12309754 1 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N N FGM59011;FIM76015;FIM79013 0 330 MG LYOPHILIZED POWDER
123097544 12309754 2 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N N FGM59011;FIM76015;FIM79013 0 350 MG LYOPHILIZED POWDER
123097544 12309754 3 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N N FGM59011;FIM76015;FIM79013 0 5 MG/KG LYOPHILIZED POWDER
123097544 12309754 4 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N N FGM59011;FIM76015;FIM79013 0 350 MG LYOPHILIZED POWDER
123097544 12309754 5 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N N FGM59011;FIM76015;FIM79013 0 400 MG LYOPHILIZED POWDER
123097544 12309754 6 PS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N N FGM59011;FIM76015;FIM79013 103772 5 MG/KG LYOPHILIZED POWDER
123097544 12309754 7 C METHOTREXATE. METHOTREXATE 1 Unknown 0 UNSPECIFIED
123097544 12309754 8 C FOLIC ACID. FOLIC ACID 1 Unknown 0 UNSPECIFIED
123097544 12309754 9 C MESALAZINE MESALAMINE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123097544 12309754 1 Colitis ulcerative
123097544 12309754 2 Colitis ulcerative
123097544 12309754 3 Colitis ulcerative
123097544 12309754 4 Colitis ulcerative
123097544 12309754 5 Colitis ulcerative
123097544 12309754 6 Colitis ulcerative

Outcome of event

Event ID CASEID OUTC COD
123097544 12309754 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123097544 12309754 Abdominal pain
123097544 12309754 Drug effect decreased
123097544 12309754 Frequent bowel movements
123097544 12309754 General physical health deterioration
123097544 12309754 Haematochezia
123097544 12309754 Off label use
123097544 12309754 Product use issue
123097544 12309754 Rectal haemorrhage
123097544 12309754 Weight decreased

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
123097544 12309754 1 20151124 0
123097544 12309754 2 20160419 0
123097544 12309754 3 20110729 0
123097544 12309754 4 20150512 0
123097544 12309754 5 20160301 0
123097544 12309754 6 201603 0