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
122950042 12295004 2 F 20110520 20160628 20160422 20160705 EXP CA-JNJFOC-20160416711 JANSSEN 15.59 YR T M Y 69.00000 KG 20160705 CN 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
122950042 12295004 1 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N FJM90015 0 800 MG LYOPHILIZED POWDER
122950042 12295004 2 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N FJM90015 0 800 MG LYOPHILIZED POWDER
122950042 12295004 3 PS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N FJM90015 103772 800 MG LYOPHILIZED POWDER
122950042 12295004 4 C SOLU-CORTEF HYDROCORTISONE SODIUM SUCCINATE 1 Intravenous (not otherwise specified) 0 200 MG UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122950042 12295004 1 Colitis ulcerative
122950042 12295004 2 Colitis ulcerative
122950042 12295004 3 Colitis ulcerative
122950042 12295004 4 Premedication

Outcome of event

Event ID CASEID OUTC COD
122950042 12295004 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122950042 12295004 Frequent bowel movements
122950042 12295004 General physical health deterioration
122950042 12295004 Off label use
122950042 12295004 Product use issue
122950042 12295004 Rectal haemorrhage

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
122950042 12295004 1 20110520 0
122950042 12295004 2 20160417 0
122950042 12295004 3 20160627 0