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
123188715 12318871 5 F 201603 20160628 20160429 20160702 EXP US-BIOGEN-2016BI00227996 BIOGEN 68.33 YR F Y 0.00000 20160702 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
123188715 12318871 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) INFUSED OVER 1 HOUR U 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
123188715 12318871 2 C NOVANTRONE MITOXANTRONE HYDROCHLORIDE 1 Unknown 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123188715 12318871 1 Multiple sclerosis
123188715 12318871 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123188715 12318871 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123188715 12318871 Cholecystitis infective
123188715 12318871 Cholelithiasis
123188715 12318871 Dyskinesia
123188715 12318871 Dysphagia
123188715 12318871 Heart rate increased
123188715 12318871 Multiple sclerosis relapse
123188715 12318871 Sepsis
123188715 12318871 Urinary tract infection

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
123188715 12318871 1 20160218 20160317 0