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
120430242 12043024 2 F 201401 20160706 20160208 20160712 EXP US-BIOGEN-2014BI014380 BIOGEN 62.03 YR M Y 0.00000 20160712 MD 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
120430242 12043024 1 PS AVONEX INTERFERON BETA-1A 1 Intramuscular 103628 30 UG SOLN FOR INJECT IN PRE-FILLED SYRINGE /wk
120430242 12043024 2 SS AVONEX INTERFERON BETA-1A 1 Unknown 103628 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120430242 12043024 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
120430242 12043024 HO
120430242 12043024 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120430242 12043024 Acute myocardial infarction
120430242 12043024 Ankle fracture
120430242 12043024 Anxiety
120430242 12043024 Depression
120430242 12043024 Femur fracture
120430242 12043024 Hypertension
120430242 12043024 Hypotonia
120430242 12043024 Muscular weakness
120430242 12043024 Personality change
120430242 12043024 Post procedural complication
120430242 12043024 Renal function test abnormal
120430242 12043024 Spinal fracture
120430242 12043024 Tobacco withdrawal symptoms

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
120430242 12043024 1 20000401 0
120430242 12043024 2 20141209 0