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
125907911 12590791 1 I 2005 20081231 20160726 20160726 EXP US-BIOGEN-2009BI000439 BIOGEN 0.00 F Y 0.00000 20160726 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
125907911 12590791 1 PS AVONEX INTERFERON BETA-1A 1 Intramuscular U 103628 30 UG SOLN FOR INJECT IN PRE-FILLED SYRINGE /wk
125907911 12590791 2 SS AVONEX INTERFERON BETA-1A 1 Intramuscular U 103628 30 UG SOLN FOR INJECT IN PRE-FILLED SYRINGE /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125907911 12590791 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
125907911 12590791 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125907911 12590791 Multiple sclerosis relapse
125907911 12590791 Muscle spasms
125907911 12590791 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
125907911 12590791 1 20040623 20060814 0
125907911 12590791 2 20061002 20090721 0