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
101102913 10110291 3 F 20150216 20150623 20140425 20150630 EXP CA-JNJFOC-20140416442 JANSSEN 51.96 YR A F Y 47.63000 KG 20150630 N 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
101102913 10110291 1 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N FAM10015 0 500 MG LYOPHILIZED POWDER
101102913 10110291 2 PS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N FAM10015 103772 500 MG LYOPHILIZED POWDER

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101102913 10110291 1 Crohn's disease
101102913 10110291 2 Crohn's disease

Outcome of event

Event ID CASEID OUTC COD
101102913 10110291 HO
101102913 10110291 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
101102913 10110291 Breast cancer
101102913 10110291 Postoperative wound infection

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
101102913 10110291 1 2009 0
101102913 10110291 2 20100107 0