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
127875621 12787562 1 I 20160902 0 20160928 20160928 DIR FDA-CTU 58.00 YR F N 0.00000 20160927 Y PH 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
127875621 12787562 1 PS AMPYRA DALFAMPRIDINE 1 Oral D D VBZ5 20181031 0 10 MG Q12H
127875621 12787562 2 C GILENYA FINGOLIMOD HYDROCHLORIDE 1 0
127875621 12787562 3 C WARFARIN WARFARIN 1 0
127875621 12787562 4 C PERCOCET ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 0
127875621 12787562 5 C PROVIGIL MODAFINIL 1 0
127875621 12787562 6 C DURAGESIC FENTANYL 1 0
127875621 12787562 7 C KLONIPIN CLONAZEPAM 1 0
127875621 12787562 8 C DITROPAN OXYBUTYNIN CHLORIDE 1 0
127875621 12787562 9 C VENTOLIN HFA ALBUTEROL SULFATE 1 0
127875621 12787562 10 C TYLENOL ACETAMINOPHEN 1 0
127875621 12787562 11 C VITAMIN B12 CYANOCOBALAMIN 1 0
127875621 12787562 12 C VITAMIN A VITAMIN A 1 0
127875621 12787562 13 C VITAMIN B-3 2 0
127875621 12787562 14 C FOLIC ACID. FOLIC ACID 1 0
127875621 12787562 15 C CHOLECALCIFEROL CHOLECALCIFEROL 1 0
127875621 12787562 16 C VITAMIN D CHOLECALCIFEROL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127875621 12787562 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127875621 12787562 Laboratory test abnormal

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

Event ID CASEID RPSR COD
127875621 12787562 HP

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127875621 12787562 1 201202 0