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
125216211 12521621 1 I 2016 20160610 20160701 20160701 PER US-BIOGEN-2016BI00258472 BIOGEN 0.00 M 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
125216211 12521621 1 PS AVONEX INTERFERON BETA-1A 1 Intramuscular U UNKNOWN 103628 SOLUTION FOR INJECTION IN PRE-FILLED PEN
125216211 12521621 2 SS AVONEX INTERFERON BETA-1A 1 Intramuscular U UNKNOWN 103628 30 UG SOLUTION FOR INJECTION IN PRE-FILLED PEN /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125216211 12521621 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125216211 12521621 Chills
125216211 12521621 Drug dose omission
125216211 12521621 Headache
125216211 12521621 Hypertension
125216211 12521621 Influenza like illness
125216211 12521621 Migraine
125216211 12521621 Monoplegia
125216211 12521621 Muscle tightness
125216211 12521621 Pain
125216211 12521621 Vision blurred

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
125216211 12521621 1 201605 0