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
125669333 12566933 3 F 20160506 20160725 20160718 20160728 EXP US-BIOGEN-2016BI00265321 BIOGEN 41.87 YR F Y 0.00000 20160728 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
125669333 12566933 1 PS 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
125669333 12566933 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
125669333 12566933 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125669333 12566933 Abdominal pain upper
125669333 12566933 Amnesia
125669333 12566933 Asthenia
125669333 12566933 Diplopia
125669333 12566933 Dizziness
125669333 12566933 Gait disturbance
125669333 12566933 General symptom
125669333 12566933 Malaise
125669333 12566933 Muscle fatigue
125669333 12566933 Nausea
125669333 12566933 Paraplegia
125669333 12566933 Vision blurred
125669333 12566933 Visual impairment

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
125669333 12566933 1 20120903 20160708 0