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
113655526 11365552 6 F 20140901 20160719 20150811 20160722 PER PHHY2014US134464 NOVARTIS 34.41 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
113655526 11365552 1 PS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral UNK UNK, QD 22527 CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113655526 11365552 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
113655526 11365552 Amnesia
113655526 11365552 Conjunctivitis
113655526 11365552 Heart rate abnormal
113655526 11365552 Lymphopenia
113655526 11365552 Neutrophil count decreased
113655526 11365552 Onychoclasis
113655526 11365552 White blood cell count decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found