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
93424694 9342469 4 F 20130606 20160906 20130611 20160912 EXP PHHY2013CA058861 NOVARTIS 51.04 YR F Y 0.00000 20160912 OT CA CA

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
93424694 9342469 1 PS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral 0.5 MG, QD Y 22527 .5 MG CAPSULE QD
93424694 9342469 2 SS TYSABRI NATALIZUMAB 1 Intravenous drip UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
93424694 9342469 1 Relapsing-remitting multiple sclerosis
93424694 9342469 2 Relapsing-remitting multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
93424694 9342469 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
93424694 9342469 Angioedema
93424694 9342469 Blood pressure decreased
93424694 9342469 Multiple sclerosis relapse
93424694 9342469 Therapeutic response decreased
93424694 9342469 Urticaria

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
93424694 9342469 1 20130606 201603 0
93424694 9342469 2 201603 0