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
125544043 12554404 3 F 2007 20160823 20160713 20160831 EXP US-BIOGEN-2016BI00261956 BIOGEN 0.00 F Y 0.00000 20160831 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
125544043 12554404 1 PS AVONEX INTERFERON BETA-1A 1 Intramuscular U 103628 30 UG SOLN FOR INJECT IN PRE-FILLED SYRINGE /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125544043 12554404 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
125544043 12554404 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125544043 12554404 Arthropod bite
125544043 12554404 Bone cyst
125544043 12554404 Device dislocation
125544043 12554404 General symptom
125544043 12554404 Hallucination
125544043 12554404 Injection site pain
125544043 12554404 Memory impairment
125544043 12554404 Nerve compression
125544043 12554404 Neuralgia
125544043 12554404 Pain
125544043 12554404 Scoliosis
125544043 12554404 Screaming
125544043 12554404 Spinal column stenosis
125544043 12554404 Visual impairment
125544043 12554404 Weight decreased

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
125544043 12554404 1 20051117 0