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
123866152 12386615 2 F 20160913 20160519 20160919 PER PHEH2016US012380 NOVARTIS 0.00 F Y 0.00000 20160919 CN COUNTRY NOT SPECIFIED 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
123866152 12386615 1 PS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Unknown UNK U 22527 CAPSULE
123866152 12386615 2 SS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral 0.5 MG, QD U F0028 22527 .5 MG CAPSULE QD
123866152 12386615 3 SS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral 0.5 MG, QOD U 22527 .5 MG CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123866152 12386615 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123866152 12386615 Inappropriate schedule of drug administration
123866152 12386615 Prescribed underdose
123866152 12386615 Urticaria

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
123866152 12386615 1 20160414 0
123866152 12386615 2 20160420 0