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
121910274 12191027 4 F 201509 20160811 20160318 20160825 EXP CA-JNJFOC-20160113530 JANSSEN 37.73 YR A F Y 67.00000 KG 20160825 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
121910274 12191027 1 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N FLM04016 0 600 MG LYOPHILIZED POWDER
121910274 12191027 2 PS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N FLM04016 103772 600 MG LYOPHILIZED POWDER

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121910274 12191027 1 Crohn's disease
121910274 12191027 2 Crohn's disease

Outcome of event

Event ID CASEID OUTC COD
121910274 12191027 OT
121910274 12191027 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121910274 12191027 Abdominal pain
121910274 12191027 Diarrhoea
121910274 12191027 Exposure during pregnancy
121910274 12191027 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
121910274 12191027 1 20160811 0
121910274 12191027 2 20120808 0