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
120854914 12085491 4 F 20160120 20160915 20160217 20160919 EXP IT-BIOGEN-2016BI00185272 BIOGEN 37.84 YR F Y 0.00000 20160919 MD IT IT

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
120854914 12085491 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) D 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
120854914 12085491 2 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) D 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
120854914 12085491 3 SS TECFIDERA DIMETHYL FUMARATE 1 Unknown D 204063 PROLONGED-RELEASE CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120854914 12085491 1 Multiple sclerosis
120854914 12085491 3 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
120854914 12085491 Multiple sclerosis
120854914 12085491 Paraparesis

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
120854914 12085491 1 20080314 20150624 0
120854914 12085491 2 20151111 20151209 0
120854914 12085491 3 20150909 20151007 0