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
89865652 8986565 2 F 20120323 20160914 20121226 20160919 EXP PHHY2012CA050252 NOVARTIS 57.94 YR F Y 0.00000 20160919 CN COUNTRY NOT SPECIFIED 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
89865652 8986565 1 PS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral 0.5 MG, QD Y 22527 .5 MG CAPSULE QD
89865652 8986565 2 SS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral UNK Y 22527 CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
89865652 8986565 1 Multiple sclerosis

Outcome of event

Event ID CASEID OUTC COD
89865652 8986565 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
89865652 8986565 Central nervous system lesion
89865652 8986565 Fatigue
89865652 8986565 Fine motor skill dysfunction
89865652 8986565 Gait disturbance
89865652 8986565 General physical health deterioration
89865652 8986565 Nausea

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
89865652 8986565 1 20120323 20120831 0
89865652 8986565 2 20130227 20140901 0