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
125796682 12579668 2 F 2016 20160721 20160721 20160729 EXP DE-SA-2016SA129864 AVENTIS 40.00 YR A F Y 0.00000 20160729 MD DE DE

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
125796682 12579668 1 PS AUBAGIO TERIFLUNOMIDE 1 Oral UNKNOWN 202992 14 MG FILM-COATED TABLET
125796682 12579668 2 SS TRIAMCINOLONE ACETONIDE. TRIAMCINOLONE ACETONIDE 1 Intrathecal UNKNOWN 0 100 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125796682 12579668 1 Multiple sclerosis
125796682 12579668 2 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
125796682 12579668 OT
125796682 12579668 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125796682 12579668 Condition aggravated
125796682 12579668 Dyspepsia
125796682 12579668 Faeces soft
125796682 12579668 Fall
125796682 12579668 Frequent bowel movements
125796682 12579668 Gait disturbance
125796682 12579668 Muscular weakness
125796682 12579668 Off label use
125796682 12579668 Tremor

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
125796682 12579668 1 201605 0
125796682 12579668 2 20160608 20160611 0