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
126101872 12610187 2 F 20160801 20160801 20160803 PER US-BIOGEN-2016BI00271534 BIOGEN 0.00 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
126101872 12610187 1 PS TECFIDERA DIMETHYL FUMARATE 1 Oral MAINTENANCE DOSE U 204063 240 MG PROLONGED-RELEASE CAPSULE BID
126101872 12610187 2 SS TECFIDERA DIMETHYL FUMARATE 1 Unknown U 204063 UNKNOWN
126101872 12610187 3 SS TECFIDERA DIMETHYL FUMARATE 1 Unknown U 204063 UNKNOWN
126101872 12610187 4 SS AVONEX INTERFERON BETA-1A 1 Unknown U 103628 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126101872 12610187 1 Multiple sclerosis
126101872 12610187 4 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126101872 12610187 General symptom
126101872 12610187 Vision blurred
126101872 12610187 Visual impairment

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
126101872 12610187 1 20130731 0
126101872 12610187 2 20130731 20130731 0
126101872 12610187 3 20130731 0