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
123626946 12362694 6 F 201604 20160809 20160512 20160812 EXP SI-BIOGEN-2016BI00235687 BIOGEN 54.00 YR F Y 0.00000 20160812 MD SI SI

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
123626946 12362694 1 PS AVONEX INTERFERON BETA-1A 1 Intramuscular U 103628 30 UG UNKNOWN /wk
123626946 12362694 2 SS AVONEX INTERFERON BETA-1A 1 Intramuscular U 103628 30 UG UNKNOWN /wk
123626946 12362694 3 SS AVONEX INTERFERON BETA-1A 1 Intramuscular U 103628 30 UG UNKNOWN /wk
123626946 12362694 4 SS AVONEX INTERFERON BETA-1A 1 Unknown U 103628 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123626946 12362694 1 Relapsing-remitting multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
123626946 12362694 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123626946 12362694 Influenza like illness
123626946 12362694 Invasive ductal breast carcinoma

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
123626946 12362694 1 2004 0
123626946 12362694 2 2010 0
123626946 12362694 3 2014 0