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
123722232 12372223 2 F 20160915 20160516 20160927 PER US-BIOGEN-2016BI00224983 BIOGEN 0.00 M Y 0.00000 20160927 CN US US

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
123722232 12372223 1 PS TECFIDERA DIMETHYL FUMARATE 1 Oral U 204063 240 MG PROLONGED-RELEASE CAPSULE BID
123722232 12372223 2 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) U 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
123722232 12372223 3 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) U 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123722232 12372223 1 Multiple sclerosis
123722232 12372223 2 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123722232 12372223 Asthenia
123722232 12372223 Diplegia
123722232 12372223 Multiple sclerosis relapse

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
123722232 12372223 1 20140522 0
123722232 12372223 2 20130625 20131209 0
123722232 12372223 3 20160115 20160311 0