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
86758943 8675894 3 F 201201 20160627 20120720 20160701 EXP PHHY2011CA101684 NOVARTIS 34.16 YR F Y 0.00000 20160701 CN CA CA

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
86758943 8675894 1 PS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral 0.5 MG, QD 22527 .5 MG CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
86758943 8675894 1 Relapsing-remitting multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
86758943 8675894 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
86758943 8675894 Abdominal pain upper
86758943 8675894 Blood pressure increased
86758943 8675894 Cardiac murmur
86758943 8675894 Chest discomfort
86758943 8675894 Chest pain
86758943 8675894 Dizziness
86758943 8675894 Dyspepsia
86758943 8675894 Fatigue
86758943 8675894 Headache
86758943 8675894 Insomnia
86758943 8675894 Migraine
86758943 8675894 Palpitations
86758943 8675894 Vertigo
86758943 8675894 Vision blurred
86758943 8675894 Visual impairment

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
86758943 8675894 1 20111115 20160520 0