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
125696051 12569605 1 I 20160704 20160714 20160719 20160719 EXP GB-JNJFOC-20160712323 JANSSEN 5.00 YR C F Y 20.00000 KG 20160719 OT GB GB

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
125696051 12569605 1 PS INFLIXIMAB, RECOMBINANT INFLIXIMAB 1 Intravenous (not otherwise specified) Y N 103772 120 DF LYOPHILIZED POWDER
125696051 12569605 2 C HYDROCORTISONE. HYDROCORTISONE 1 Unknown 0 UNSPECIFIED
125696051 12569605 3 C CHLORPHENAMINE CHLORPHENIRAMINE MALEATE 1 Unknown 0 UNSPECIFIED
125696051 12569605 4 C METHOTREXATE. METHOTREXATE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125696051 12569605 1 Juvenile idiopathic arthritis
125696051 12569605 2 Premedication
125696051 12569605 3 Premedication

Outcome of event

Event ID CASEID OUTC COD
125696051 12569605 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125696051 12569605 Anaphylactic reaction
125696051 12569605 Chest pain
125696051 12569605 Infusion related reaction

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
125696051 12569605 1 20160704 20160704 0