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
126097011 12609701 1 I 20160624 0 20160729 20160729 DIR 39.00 YR F N 0.00000 20160728 Y PH 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
126097011 12609701 1 PS AMPYRA DALFAMPRIDINE 1 Oral D D TCNV 20180430 0 10 MG Q12H
126097011 12609701 3 C GLATOPA GLATIRAMER ACETATE 1 0
126097011 12609701 5 C NEURONTIN GABAPENTIN 1 0
126097011 12609701 7 C PROVIGIL MODAFINIL 1 0
126097011 12609701 9 C SYMMETREL AMANTADINE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126097011 12609701 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126097011 12609701 Laboratory test abnormal
126097011 12609701 Platelet count increased
126097011 12609701 Protein urine
126097011 12609701 Urine leukocyte esterase positive

Reporting Sources (this data is often not reported and may therefore be missing here)

Event ID CASEID RPSR COD
126097011 12609701 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126097011 12609701 1 201401 0