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
119903454 11990345 4 F 20160115 20160712 20160202 20160715 EXP CA-BIOGEN-2016BI00181742 BIOGEN 52.60 YR F Y 0.00000 20160715 MD CA CA

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
119903454 11990345 1 PS FAMPYRA DALFAMPRIDINE 1 Oral 22250 10 MG PROLONGED-RELEASE TABLET BID
119903454 11990345 2 SS AVONEX INTERFERON BETA-1A 1 Intramuscular 103628 30 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119903454 11990345 1 Gait disturbance
119903454 11990345 2 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
119903454 11990345 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
119903454 11990345 Dysphagia
119903454 11990345 Intervertebral disc protrusion
119903454 11990345 Musculoskeletal disorder
119903454 11990345 Pain

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
119903454 11990345 1 20140817 0
119903454 11990345 2 20121101 0