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
112749315 11274931 5 F 20140716 20160926 20150716 20160929 PER PHHY2015US041048 NOVARTIS 53.45 YR F Y 0.00000 20160929 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
112749315 11274931 1 PS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral UNK 22527 CAPSULE
112749315 11274931 2 C ESTRACE ESTRADIOL 1 Unknown 0.01 %, UNK 0 .01 PCT
112749315 11274931 3 C ESTRACE ESTRADIOL 1 Unknown 0.01 %, UNK 0 .01 PCT

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112749315 11274931 1 Multiple sclerosis
112749315 11274931 2 Atrophic vulvovaginitis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
112749315 11274931 Lymphocyte count decreased
112749315 11274931 Papilloma viral infection

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
112749315 11274931 2 20140918 20141016 0
112749315 11274931 3 20150107 0