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
127721701 12772170 1 I 20140401 20160916 20160922 20160922 EXP GB-JNJFOC-20160917640 JANSSEN 14.00 YR T M Y 46.40000 KG 20160922 MD 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
127721701 12772170 1 PS INFLIXIMAB, RECOMBINANT INFLIXIMAB 1 Intravenous (not otherwise specified) N 103772 6 DF LYOPHILIZED POWDER
127721701 12772170 2 C IBUPROFEN. IBUPROFEN 1 Unknown D 0 UNSPECIFIED
127721701 12772170 3 C PARACETAMOL ACETAMINOPHEN 1 Unknown D 0 UNSPECIFIED
127721701 12772170 4 C AMITRIPTYLINE AMITRIPTYLINE 1 Unknown D 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127721701 12772170 1 Juvenile idiopathic arthritis

Outcome of event

Event ID CASEID OUTC COD
127721701 12772170 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127721701 12772170 Off label use
127721701 12772170 Pancreatitis
127721701 12772170 Product use issue

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
127721701 12772170 1 20140401 0