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
121684253 12168425 3 F 201511 20160707 20160310 20160719 EXP DE-BIOGEN-2015BI082491 BIOGEN 43.23 YR F Y 0.00000 20160719 MD DE DE

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
121684253 12168425 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) Y 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
121684253 12168425 2 C COPAXONE GLATIRAMER ACETATE 1 Unknown 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121684253 12168425 1 Multiple sclerosis
121684253 12168425 2 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
121684253 12168425 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121684253 12168425 Multiple sclerosis relapse
121684253 12168425 Progressive multifocal leukoencephalopathy

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
121684253 12168425 1 200810 20150227 0
121684253 12168425 2 201508 0