The Safety Rates Drug Report

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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
125631682 12563168 2 F 20160804 20160715 20160811 PER PHEH2016US017280 NOVARTIS 0.00 F Y 0.00000 20160811 CN 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
125631682 12563168 1 PS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral 0.5 MG, QD U 22527 .5 MG CAPSULE QD
125631682 12563168 2 SS AMPYRA DALFAMPRIDINE 1 Oral 10 MG, Q12H U 0 10 MG Q12H
125631682 12563168 3 C MULTI VIT 2 Unknown UNK U 0
125631682 12563168 4 C VITAMIN D3 CHOLECALCIFEROL 1 Unknown U 0
125631682 12563168 5 C IRON IRON 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125631682 12563168 1 Multiple sclerosis
125631682 12563168 2 Multiple sclerosis
125631682 12563168 3 Product used for unknown indication
125631682 12563168 4 Product used for unknown indication
125631682 12563168 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125631682 12563168 Multiple sclerosis relapse

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
125631682 12563168 1 201103 0