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
125257721 12525772 1 I 20160629 20160705 20160705 PER US-BIOGEN-2016BI00260107 BIOGEN 0.00 F Y 0.00000 20160705 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
125257721 12525772 1 PS AVONEX INTERFERON BETA-1A 1 Unknown Y 103628 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125257721 12525772 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125257721 12525772 Drug intolerance
125257721 12525772 Eye disorder
125257721 12525772 Fall
125257721 12525772 Foreign body
125257721 12525772 Malaise
125257721 12525772 Memory impairment
125257721 12525772 Multiple sclerosis relapse
125257721 12525772 Oesophageal disorder
125257721 12525772 Subcutaneous abscess
125257721 12525772 Upper limb fracture

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
125257721 12525772 1 20030829 0