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
101455808 10145580 8 F 20140226 20160928 20140501 20160930 EXP US-JNJFOC-20140418714 JANSSEN 13.11 YR C F Y 41.10000 KG 20160930 MD US US

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
101455808 10145580 1 PS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) D N 103772 LYOPHILIZED POWDER
101455808 10145580 2 C HUMIRA ADALIMUMAB 1 Unknown D 0 UNSPECIFIED
101455808 10145580 3 C IMURAN AZATHIOPRINE 1 Unknown D 0 UNSPECIFIED
101455808 10145580 4 C MULTIVITAMINS VITAMINS 1 Unknown D 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101455808 10145580 1 Inflammatory bowel disease

Outcome of event

Event ID CASEID OUTC COD
101455808 10145580 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
101455808 10145580 Crohn's disease

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
101455808 10145580 1 20091210 0
101455808 10145580 2 20130401 20140408 0