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
126096851 12609685 1 I 20160726 0 20160729 20160729 DIR 50.00 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
126096851 12609685 1 PS AMPYRA DALFAMPRIDINE 1 Oral D D TCNV 20180430 0 10 MG Q12H
126096851 12609685 3 C RITUXAN RITUXIMAB 1 0
126096851 12609685 5 C TRAZODONE TRAZODONE HYDROCHLORIDE 1 0
126096851 12609685 7 C LIZANIDINE 2 0
126096851 12609685 9 C MODAFINIL. MODAFINIL 1 0
126096851 12609685 11 C BUPROPION. BUPROPION 1 0
126096851 12609685 13 C LEVOTHYROXINE. LEVOTHYROXINE 1 0
126096851 12609685 15 C CABERGOLINE. CABERGOLINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126096851 12609685 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126096851 12609685 B-lymphocyte count decreased
126096851 12609685 CD4 lymphocytes decreased
126096851 12609685 Laboratory test abnormal
126096851 12609685 T-lymphocyte count increased

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
126096851 12609685 1 201602 0