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
126975681 12697568 1 I 20160816 20160830 20160830 EXP US-ACORDA-ACO_127590_2016 ACORDA 65.00 YR F Y 0.00000 20160830 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
126975681 12697568 1 PS AMPYRA DALFAMPRIDINE 1 Unknown UNK U U 22250 TABLET
126975681 12697568 2 SS AMPYRA DALFAMPRIDINE 1 Unknown UNK U U 22250 TABLET
126975681 12697568 3 C REBIF INTERFERON BETA-1A 1 Unknown UNK U 0
126975681 12697568 4 C REBIF INTERFERON BETA-1A 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126975681 12697568 1 Product used for unknown indication
126975681 12697568 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126975681 12697568 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126975681 12697568 Abasia
126975681 12697568 Multiple sclerosis
126975681 12697568 Urinary tract infection

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
126975681 12697568 1 2013 0
126975681 12697568 3 2013 0