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
114717192 11471719 2 F 20130219 20160729 20150908 20160802 EXP CA-JNJFOC-20150310054 JANSSEN 45.62 YR A F Y 62.40000 KG 20160802 OT 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
114717192 11471719 1 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N N 0 400 MG LYOPHILIZED POWDER
114717192 11471719 2 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N N 0 400 MG LYOPHILIZED POWDER
114717192 11471719 3 PS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N N 103772 400 MG LYOPHILIZED POWDER
114717192 11471719 4 SS METHOTREXATE. METHOTREXATE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114717192 11471719 1 Rheumatoid arthritis
114717192 11471719 2 Rheumatoid arthritis
114717192 11471719 3 Rheumatoid arthritis
114717192 11471719 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
114717192 11471719 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
114717192 11471719 Foot operation
114717192 11471719 Off label use
114717192 11471719 Pneumonia legionella
114717192 11471719 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
114717192 11471719 1 20130219 0
114717192 11471719 2 201503 0
114717192 11471719 3 20130519 0