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
103439158 10343915 8 F 20140201 20160901 20140727 20160906 EXP PHHY2014IT070852 NOVARTIS 43.76 YR M Y 0.00000 20160906 OT IT IT

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
103439158 10343915 1 PS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral 0.5 MG, QD 67.4690018 MG Y 22527 .5 MG CAPSULE QD
103439158 10343915 2 SS SATIVEX NABIXIMOLS 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
103439158 10343915 1 Multiple sclerosis
103439158 10343915 2 Muscle spasticity

Outcome of event

Event ID CASEID OUTC COD
103439158 10343915 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
103439158 10343915 Alanine aminotransferase increased
103439158 10343915 Aphasia
103439158 10343915 Blood pressure systolic increased
103439158 10343915 Confusional state
103439158 10343915 Depression
103439158 10343915 Fatigue
103439158 10343915 Headache
103439158 10343915 High density lipoprotein increased
103439158 10343915 Influenza like illness

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
103439158 10343915 1 20131119 20140410 0
103439158 10343915 2 20141106 0