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
124470944 12447094 4 F 20160623 20160608 20160707 EXP US-ACORDA-ACO_124938_2016 ACORDA 0.00 F Y 0.00000 20160707 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
124470944 12447094 1 PS AMPYRA DALFAMPRIDINE 1 Oral 10 MG, BID U U 22250 10 MG TABLET BID
124470944 12447094 2 SS AMPYRA DALFAMPRIDINE 1 U U 22250 TABLET
124470944 12447094 3 SS Steroids UNSPECIFIED INGREDIENT 1 UNK U U 0
124470944 12447094 4 C TECFIDERA DIMETHYL FUMARATE 1 U U 0
124470944 12447094 5 C TYSABRI NATALIZUMAB 1 Subcutaneous UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124470944 12447094 1 Gait disturbance
124470944 12447094 2 Multiple sclerosis
124470944 12447094 3 Product used for unknown indication
124470944 12447094 4 Product used for unknown indication
124470944 12447094 5 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
124470944 12447094 HO
124470944 12447094 DE
124470944 12447094 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124470944 12447094 Decubitus ulcer
124470944 12447094 Headache
124470944 12447094 Respiratory failure
124470944 12447094 Stress
124470944 12447094 Weight increased
124470944 12447094 White blood cell count decreased

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
124470944 12447094 1 20140905 0
124470944 12447094 5 20140905 0