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
124396143 12439614 3 F 2010 20160627 20160606 20160701 EXP US-BIOGEN-2014BI103351 BIOGEN 68.60 YR F Y 0.00000 20160701 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
124396143 12439614 1 PS AVONEX INTERFERON BETA-1A 1 Intramuscular U 103628 30 UG SOLN FOR INJECT IN PRE-FILLED SYRINGE /wk
124396143 12439614 2 SS AVONEX INTERFERON BETA-1A 1 Intramuscular U 103628 30 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN /wk
124396143 12439614 3 SS AVONEX INTERFERON BETA-1A 1 Intramuscular U 103628 30 UG UNKNOWN /wk
124396143 12439614 4 SS AVONEX INTERFERON BETA-1A 1 Intramuscular U 103628 30 UG SOLN FOR INJECT IN PRE-FILLED SYRINGE /wk
124396143 12439614 5 SS AVONEX INTERFERON BETA-1A 1 Intramuscular U 103628 30 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124396143 12439614 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
124396143 12439614 HO
124396143 12439614 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124396143 12439614 Anxiety
124396143 12439614 Blindness
124396143 12439614 Cerebrovascular accident
124396143 12439614 Myocardial infarction

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
124396143 12439614 1 2005 0
124396143 12439614 2 20100107 0
124396143 12439614 3 20130920 0
124396143 12439614 4 2016 0
124396143 12439614 5 201603 0