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
121278902 12127890 2 F 20141031 20160926 20160229 20160930 EXP US-BIOGEN-2014BI122907 BIOGEN 54.36 YR F Y 0.00000 20160930 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
121278902 12127890 1 PS AVONEX INTERFERON BETA-1A 1 Intramuscular 103628 30 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN /wk
121278902 12127890 2 SS AVONEX INTERFERON BETA-1A 1 Unknown 103628 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121278902 12127890 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
121278902 12127890 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
121278902 12127890 Coma
121278902 12127890 Gait disturbance
121278902 12127890 Memory impairment
121278902 12127890 Multiple sclerosis relapse
121278902 12127890 Pain
121278902 12127890 Urinary retention
121278902 12127890 Urosepsis

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
121278902 12127890 1 20130131 0
121278902 12127890 2 20130601 0