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
125408304 12540830 4 F 20160718 20160708 20160721 EXP US-BIOGEN-2016BI00261634 BIOGEN 0.00 F Y 0.00000 20160721 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
125408304 12540830 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
125408304 12540830 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
125408304 12540830 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125408304 12540830 Asthenia
125408304 12540830 Bipolar disorder
125408304 12540830 Cardiac failure congestive
125408304 12540830 Cognitive disorder
125408304 12540830 Confusional state
125408304 12540830 Dizziness
125408304 12540830 Hydrocephalus
125408304 12540830 Psychotic disorder
125408304 12540830 Shunt malfunction
125408304 12540830 Therapy non-responder

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
125408304 12540830 1 2000 2015 0