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
114329296 11432929 6 F 20150427 20160719 20150828 20160722 PER PHHY2015US097755 NOVARTIS 56.34 YR F Y 0.00000 20160722 MD US 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
114329296 11432929 1 PS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral UNK, QD 22527 CAPSULE QD
114329296 11432929 2 C DULOXETINE. DULOXETINE 1 Unknown Y 0
114329296 11432929 3 C DULOXETINE. DULOXETINE 1 Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114329296 11432929 1 Multiple sclerosis
114329296 11432929 2 Depression
114329296 11432929 3 Pain

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
114329296 11432929 Balance disorder
114329296 11432929 Decreased appetite
114329296 11432929 Dysphagia
114329296 11432929 Fatigue
114329296 11432929 Headache
114329296 11432929 Hot flush
114329296 11432929 Irritability
114329296 11432929 Lymphopenia
114329296 11432929 Micturition urgency
114329296 11432929 Muscular weakness
114329296 11432929 Nasal congestion
114329296 11432929 Nausea
114329296 11432929 Skin discolouration
114329296 11432929 Urinary hesitation
114329296 11432929 Weight 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
114329296 11432929 2 20150427 20150514 0