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
126633891 12663389 1 I 20160728 20160804 20160818 20160818 EXP US-ACORDA-ACO_127040_2016 ACORDA 0.00 F Y 47.62000 KG 20160818 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
126633891 12663389 1 PS AMPYRA DALFAMPRIDINE 1 Oral 10 MG, BID Y U 22250 10 MG TABLET BID
126633891 12663389 2 SS AMPYRA DALFAMPRIDINE 1 Oral 10MG, BID Y U 22250 TABLET
126633891 12663389 3 SS AMPYRA DALFAMPRIDINE 1 Oral 10 MG , BID Y U 22250 TABLET
126633891 12663389 4 C CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 UNK U 0
126633891 12663389 5 C Rituximab RITUXIMAB 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126633891 12663389 1 Gait disturbance
126633891 12663389 2 Multiple sclerosis
126633891 12663389 4 Product used for unknown indication
126633891 12663389 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126633891 12663389 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
126633891 12663389 Abasia
126633891 12663389 Condition aggravated
126633891 12663389 Confusional state
126633891 12663389 Disturbance in attention
126633891 12663389 Gait disturbance
126633891 12663389 Insomnia
126633891 12663389 Trigeminal neuralgia
126633891 12663389 Wheelchair user

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
126633891 12663389 1 2010 0
126633891 12663389 3 20160729 20160801 0
126633891 12663389 4 201106 201112 0
126633891 12663389 5 2014 0