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
124920413 12492041 3 F 201511 20160725 20160623 20160808 EXP US-ACORDA-ACO_125276_2016 ACORDA 0.00 F Y 0.00000 20160808 OT 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
124920413 12492041 1 PS AMPYRA DALFAMPRIDINE 1 Oral 10 MG, BID 22250 10 MG TABLET BID
124920413 12492041 2 C BUPROPION. BUPROPION 1 Oral 150 MG, BID U 0 150 MG BID
124920413 12492041 3 C TYSABRI NATALIZUMAB 1 Intravenous (not otherwise specified) 250 MG, MONTHLY U 0 250 MG /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124920413 12492041 1 Multiple sclerosis
124920413 12492041 2 Product used for unknown indication
124920413 12492041 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124920413 12492041 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124920413 12492041 Abdominal discomfort
124920413 12492041 Depression
124920413 12492041 Eye disorder
124920413 12492041 Multiple sclerosis relapse

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
124920413 12492041 2 201601 0
124920413 12492041 3 2015 0