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
125278142 12527814 2 F 20160622 20160705 20160705 20160719 EXP US-ACORDA-ACO_125589_2016 ACORDA 69.80 YR M Y 73.47000 KG 20160719 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
125278142 12527814 1 PS AMPYRA DALFAMPRIDINE 1 Oral 10 MG, BID 22250 10 MG TABLET BID
125278142 12527814 2 C Other lipid modifying agents UNSPECIFIED INGREDIENT 1 Unknown UNK U 0
125278142 12527814 3 C Other therapeutic products UNSPECIFIED INGREDIENT 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125278142 12527814 1 Gait disturbance
125278142 12527814 2 Product used for unknown indication
125278142 12527814 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125278142 12527814 Abasia
125278142 12527814 Dizziness
125278142 12527814 Headache
125278142 12527814 Muscular weakness
125278142 12527814 Nausea

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
125278142 12527814 1 20160622 0