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
125197281 12519728 1 I 20160622 20160701 20160701 PER US-BIOGEN-2016BI00256877 BIOGEN 0.00 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
125197281 12519728 1 PS AVONEX INTERFERON BETA-1A 1 Intramuscular 103628 30 UG SOLN FOR INJECT IN PRE-FILLED SYRINGE /wk
125197281 12519728 2 SS AVONEX INTERFERON BETA-1A 1 Intramuscular 103628 30 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN /wk
125197281 12519728 3 SS AVONEX INTERFERON BETA-1A 1 Intramuscular 103628 30 UG SOLN FOR INJECT IN PRE-FILLED SYRINGE /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125197281 12519728 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125197281 12519728 Fall

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
125197281 12519728 1 201011 201209 0
125197281 12519728 2 201209 201308 0
125197281 12519728 3 201308 0