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
123789802 12378980 2 F 201403 20160701 20160517 20160708 EXP PT-BIOGEN-2016BI00237781 BIOGEN 30.27 YR F Y 0.00000 20160708 MD PT PT

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
123789802 12378980 1 PS AVONEX INTERFERON BETA-1A 1 Intramuscular N 103628 30 UG UNKNOWN /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123789802 12378980 1 Clinically isolated syndrome

Outcome of event

Event ID CASEID OUTC COD
123789802 12378980 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123789802 12378980 Drug-induced liver injury
123789802 12378980 Multiple sclerosis relapse

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
123789802 12378980 1 20150717 0