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
125190732 12519073 2 F 20160804 20160701 20160811 EXP US-BIOGEN-2016BI00258177 BIOGEN 0.00 M Y 0.00000 20160811 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
125190732 12519073 1 PS TYSABRI NATALIZUMAB 1 Unknown U 125104 CONCENTRATE FOR SOLUTION FOR INFUSION
125190732 12519073 2 SS AVONEX INTERFERON BETA-1A 1 Unknown U 103628 UNKNOWN
125190732 12519073 3 SS AVONEX INTERFERON BETA-1A 1 Unknown U 103628 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125190732 12519073 1 Multiple sclerosis
125190732 12519073 2 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125190732 12519073 Hypoacusis
125190732 12519073 Memory impairment

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
125190732 12519073 1 20140417 20141002 0
125190732 12519073 2 20131021 0
125190732 12519073 3 20131118 0