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
124848372 12484837 2 F 20160722 20160621 20160728 EXP FR-BIOGEN-2016BI00253186 BIOGEN 0.00 M Y 0.00000 20160728 MD FR FR

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
124848372 12484837 1 PS AVONEX INTERFERON BETA-1A 1 Intramuscular U 103628 30 UG UNKNOWN /wk
124848372 12484837 2 SS AVONEX INTERFERON BETA-1A 1 Unknown U 103628 UNKNOWN
124848372 12484837 3 SS AVONEX INTERFERON BETA-1A 1 Unknown U 103628 30 UG UNKNOWN /wk
124848372 12484837 4 C RIVOTRIL CLONAZEPAM 1 Unknown 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124848372 12484837 1 Relapsing-remitting multiple sclerosis
124848372 12484837 4 Multiple sclerosis relapse

Outcome of event

Event ID CASEID OUTC COD
124848372 12484837 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124848372 12484837 Depression
124848372 12484837 Drug ineffective
124848372 12484837 Multiple sclerosis relapse
124848372 12484837 Secondary progressive multiple sclerosis

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
124848372 12484837 1 199706 0
124848372 12484837 2 2007 0
124848372 12484837 3 20080115 20090615 0