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
93236932 9323693 2 F 20160711 20160712 20130603 20160718 EXP PHHY2013IL029103 NOVARTIS 41.22 YR F Y 0.00000 20160719 CN COUNTRY NOT SPECIFIED 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
93236932 9323693 1 PS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral 0.5 MG, QD U 22527 .5 MG CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
93236932 9323693 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
93236932 9323693 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
93236932 9323693 Asthenia
93236932 9323693 Dysuria
93236932 9323693 Gait disturbance
93236932 9323693 Hypoaesthesia
93236932 9323693 Limb discomfort
93236932 9323693 Multiple sclerosis relapse
93236932 9323693 Muscular weakness
93236932 9323693 Nuclear magnetic resonance imaging abnormal
93236932 9323693 Tinnitus
93236932 9323693 Vertigo

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
93236932 9323693 1 20121016 0