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
98252263 9825226 3 F 20120122 20160825 20140117 20160829 EXP FR-JNJFOC-20140106846 JANSSEN 82.00 YR E M Y 90.00000 KG 20160829 MD FR FR

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
98252263 9825226 1 SS INFLIXIMAB, RECOMBINANT INFLIXIMAB 1 Intravenous (not otherwise specified) U U 0 10 MG/KG LYOPHILIZED POWDER
98252263 9825226 2 PS INFLIXIMAB, RECOMBINANT INFLIXIMAB 1 Intravenous (not otherwise specified) U U 103772 10 MG/KG LYOPHILIZED POWDER
98252263 9825226 3 SS HUMIRA ADALIMUMAB 1 Unknown U 0 60 MG UNSPECIFIED
98252263 9825226 4 SS HUMIRA ADALIMUMAB 1 Unknown U 0 60 MG UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98252263 9825226 1 Rheumatoid arthritis
98252263 9825226 2 Colitis ulcerative
98252263 9825226 3 Colitis ulcerative
98252263 9825226 4 Polyarthritis

Outcome of event

Event ID CASEID OUTC COD
98252263 9825226 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
98252263 9825226 Pneumonia

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
98252263 9825226 1 20101207 20101229 0
98252263 9825226 2 20101207 20101229 0
98252263 9825226 3 20110217 0
98252263 9825226 4 20110217 0