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
125433481 12543348 1 I 200802 20140924 20160711 20160711 EXP US-BIOGEN-2014BI101221 BIOGEN 57.13 YR F Y 0.00000 20160711 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
125433481 12543348 1 PS AVONEX INTERFERON BETA-1A 1 Intramuscular 103628 30 UG UNKNOWN /wk
125433481 12543348 2 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
125433481 12543348 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
125433481 12543348 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125433481 12543348 Blindness
125433481 12543348 Headache
125433481 12543348 Influenza like illness

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
125433481 12543348 1 20100310 0
125433481 12543348 2 2008 0