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
125494502 12549450 2 F 20160630 20160801 20160712 20160803 EXP US-BIOGEN-2016BI00263783 BIOGEN 39.65 YR M Y 0.00000 20160803 CN 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
125494502 12549450 1 PS PLEGRIDY PEGINTERFERON BETA-1A 1 Unknown U 125499 UNKNOWN
125494502 12549450 2 SS PLEGRIDY PEGINTERFERON BETA-1A 1 Unknown U 125499 UNKNOWN
125494502 12549450 3 SS TYSABRI NATALIZUMAB 1 Unknown 125104 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125494502 12549450 1 Multiple sclerosis
125494502 12549450 3 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
125494502 12549450 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125494502 12549450 Blood glucose increased
125494502 12549450 Headache
125494502 12549450 Influenza like illness
125494502 12549450 Loss of control of legs
125494502 12549450 Pain in extremity

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
125494502 12549450 1 20160613 20160630 0
125494502 12549450 3 20130213 20160429 0