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
101023673 10102367 3 F 20131105 20160706 20140424 20160713 EXP PHHY2013IE126927 NOVARTIS 43.01 YR F Y 0.00000 20160714 CN COUNTRY NOT SPECIFIED IE

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
101023673 10102367 1 PS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral 0.5 MG, QD 64 MG 22527 .5 MG CAPSULE QD
101023673 10102367 2 SS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral 0.5 MG, QD 64 MG 22527 .5 MG CAPSULE QD
101023673 10102367 3 C LOSARTAN. LOSARTAN 1 Unknown 50 MG, QD U 0 50 MG QD
101023673 10102367 4 C PERINDOPRIL PERINDOPRIL 1 Unknown 5 MG, QD U 0 5 MG QD
101023673 10102367 5 C TETRACYCLINE TETRACYCLINE 1 Unknown 300 MG, QD U 0 300 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
101023673 10102367 1 Relapsing-remitting multiple sclerosis
101023673 10102367 3 Product used for unknown indication
101023673 10102367 4 Product used for unknown indication
101023673 10102367 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
101023673 10102367 HO
101023673 10102367 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
101023673 10102367 Hypoaesthesia
101023673 10102367 Macular oedema
101023673 10102367 Multiple sclerosis relapse
101023673 10102367 Optic neuritis
101023673 10102367 Uveitis
101023673 10102367 Vision blurred

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
101023673 10102367 1 20130703 20131106 0
101023673 10102367 2 20140110 0