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
123430463 12343046 3 F 201406 20160630 20160506 20160707 EXP US-BIOGEN-2015BI062238 BIOGEN 55.18 YR M Y 0.00000 20160707 OT 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
123430463 12343046 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) Y 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
123430463 12343046 2 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) Y 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
123430463 12343046 3 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) INFUSED IN 1 HOUR Y 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123430463 12343046 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
123430463 12343046 OT
123430463 12343046 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123430463 12343046 Arthritis infective
123430463 12343046 Central venous catheterisation
123430463 12343046 Drug dose omission
123430463 12343046 Gait disturbance
123430463 12343046 Knee arthroplasty
123430463 12343046 Patella fracture
123430463 12343046 Staphylococcal infection
123430463 12343046 Visual 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
123430463 12343046 2 20140401 20150307 0
123430463 12343046 3 20160428 0