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
123862012 12386201 2 F 201411 20160627 20160519 20160701 EXP US-BIOGEN-2016BI00239060 BIOGEN 58.63 YR F Y 0.00000 20160701 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
123862012 12386201 1 PS TYSABRI NATALIZUMAB 1 Unknown U 125104 UNKNOWN
123862012 12386201 2 SS TYSABRI NATALIZUMAB 1 Unknown U 125104 UNKNOWN
123862012 12386201 3 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) U 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123862012 12386201 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
123862012 12386201 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123862012 12386201 Localised infection
123862012 12386201 Pneumonia

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
123862012 12386201 1 20080715 20100517 0
123862012 12386201 2 201411 0
123862012 12386201 3 20080415 0