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
125177913 12517791 3 F 20160627 20160809 20160630 20160817 EXP US-BIOGEN-2016BI00259545 BIOGEN 27.26 YR F Y 0.00000 20160817 MD 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
125177913 12517791 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) INFUSED OVER 1 HOUR 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
125177913 12517791 2 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) INFUSED OVER 1 HOUR 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125177913 12517791 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
125177913 12517791 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125177913 12517791 Arthralgia
125177913 12517791 Gait disturbance
125177913 12517791 Hypoaesthesia

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
125177913 12517791 1 20101105 20141218 0
125177913 12517791 2 20160114 0