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
125683852 12568385 2 F 20160830 20160718 20160908 EXP US-BIOGEN-2016BI00264617 BIOGEN 0.00 F Y 0.00000 20160908 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
125683852 12568385 1 PS TYSABRI NATALIZUMAB 1 Unknown 125104 UNKNOWN
125683852 12568385 2 SS TYSABRI NATALIZUMAB 1 Unknown 125104 UNKNOWN
125683852 12568385 3 SS TYSABRI NATALIZUMAB 1 Unknown 125104 UNKNOWN
125683852 12568385 4 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
125683852 12568385 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
125683852 12568385 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125683852 12568385 Death

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
125683852 12568385 1 20070806 20100316 0
125683852 12568385 2 20100630 20140321 0
125683852 12568385 3 20140724 0
125683852 12568385 4 20160310 0