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
112429392 11242939 2 F 201411 20160811 20150707 20160818 EXP PHHY2015PT035415 NOVARTIS 27.32 YR F Y 0.00000 20160818 OT PT PT

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
112429392 11242939 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
112429392 11242939 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
112429392 11242939 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
112429392 11242939 Blood cholesterol increased
112429392 11242939 Blood triglycerides increased
112429392 11242939 Dysgeusia
112429392 11242939 Hypoaesthesia oral
112429392 11242939 Insomnia
112429392 11242939 Lymphocyte count decreased
112429392 11242939 Multiple sclerosis relapse
112429392 11242939 Muscular weakness
112429392 11242939 Musculoskeletal pain
112429392 11242939 Oedema
112429392 11242939 Urinary incontinence
112429392 11242939 Urinary tract infection
112429392 11242939 Vitamin D decreased
112429392 11242939 White blood cell count decreased

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
112429392 11242939 1 20140528 0