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
111251356 11125135 6 F 20150326 20160828 20150520 20160901 EXP PHHY2015IL038564 NOVARTIS 64.46 YR F Y 0.00000 20160901 CN IL IL

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
111251356 11125135 1 PS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral 0.5 MG, QD U S0097 22527 .5 MG CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
111251356 11125135 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
111251356 11125135 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
111251356 11125135 Balance disorder
111251356 11125135 Blood glucose increased
111251356 11125135 Concomitant disease aggravated
111251356 11125135 Dizziness
111251356 11125135 Ear infection
111251356 11125135 Facial pain
111251356 11125135 Fatigue
111251356 11125135 Gingivitis
111251356 11125135 Headache
111251356 11125135 Tinnitus
111251356 11125135 Vertigo
111251356 11125135 Vomiting

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
111251356 11125135 1 20150208 0