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
118006163 11800616 3 F 20141116 20160822 20151204 20160829 PER PHHY2015US056003 NOVARTIS 52.57 YR F Y 0.00000 20160829 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
118006163 11800616 1 PS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral 22527 CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118006163 11800616 1 Multiple sclerosis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
118006163 11800616 Alopecia
118006163 11800616 Arthralgia
118006163 11800616 Asthenia
118006163 11800616 Balance disorder
118006163 11800616 Blood creatine increased
118006163 11800616 Concomitant disease aggravated
118006163 11800616 Contusion
118006163 11800616 Diarrhoea
118006163 11800616 Eye pain
118006163 11800616 Fall
118006163 11800616 Fatigue
118006163 11800616 Headache
118006163 11800616 Lymphocyte count decreased
118006163 11800616 Nausea
118006163 11800616 Neutrophil count decreased
118006163 11800616 Pain in extremity
118006163 11800616 Paraesthesia
118006163 11800616 Rotator cuff syndrome
118006163 11800616 Visual impairment

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

no results found

Therapies reported

no results found