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
118859925 11885992 5 F 201508 20160705 20160104 20160712 EXP US-BIOGEN-2015BI122401 BIOGEN 40.39 YR F Y 0.00000 20160712 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
118859925 11885992 1 PS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) INFUSED OVER 1 HOUR N 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION
118859925 11885992 2 SS TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) N 125104 300 MG CONCENTRATE FOR SOLUTION FOR INFUSION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118859925 11885992 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
118859925 11885992 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
118859925 11885992 Cervix carcinoma
118859925 11885992 Drug effect decreased
118859925 11885992 Gait disturbance
118859925 11885992 Human papilloma virus test positive

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
118859925 11885992 2 20091008 20160412 0