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
124812093 12481209 3 F 201508 20160712 20160620 20160719 EXP US-BIOGEN-2016BI00253126 BIOGEN 59.14 YR F Y 0.00000 20160719 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
124812093 12481209 1 PS AVONEX INTERFERON BETA-1A 1 Intramuscular 103628 30 UG SOLN FOR INJECT IN PRE-FILLED SYRINGE /wk
124812093 12481209 2 C GABAPENTIN. GABAPENTIN 1 Oral 0 800 MG TABLETS TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124812093 12481209 1 Multiple sclerosis
124812093 12481209 2 Optic nerve injury

Outcome of event

Event ID CASEID OUTC COD
124812093 12481209 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124812093 12481209 Hypoaesthesia
124812093 12481209 Multiple sclerosis relapse
124812093 12481209 Paraesthesia
124812093 12481209 Sensory loss

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
124812093 12481209 1 19981001 0
124812093 12481209 2 2004 0