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
124719682 12471968 2 F 2016 20160811 20160616 20160816 EXP CA-JNJFOC-20160313361 JANSSEN 46.65 YR A F Y 51.00000 KG 20160816 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
124719682 12471968 1 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N 0 300 MG LYOPHILIZED POWDER
124719682 12471968 2 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N 0 300 MG LYOPHILIZED POWDER
124719682 12471968 3 PS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N 103772 300 MG LYOPHILIZED POWDER

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124719682 12471968 1 Colitis ulcerative
124719682 12471968 2 Colitis ulcerative
124719682 12471968 3 Colitis ulcerative

Outcome of event

Event ID CASEID OUTC COD
124719682 12471968 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124719682 12471968 Arthralgia
124719682 12471968 Chromaturia
124719682 12471968 Infection
124719682 12471968 Influenza
124719682 12471968 Pneumonia
124719682 12471968 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
124719682 12471968 1 20140605 0
124719682 12471968 2 20160511 0
124719682 12471968 3 20160118 0