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
125309101 12530910 1 I 20160628 20160706 20160706 EXP PHFR2016GB005352 SANDOZ 0.00 F Y 0.00000 20160706 CN COUNTRY NOT SPECIFIED GB

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
125309101 12530910 1 SS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral 0.5 MG, QD U 0 .5 MG CAPSULE QD
125309101 12530910 2 PS AMITRIPTYLINE AMITRIPTYLINE 1 Unknown 5 MG, QHS U 85966 5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125309101 12530910 1 Multiple sclerosis
125309101 12530910 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125309101 12530910 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125309101 12530910 Diplopia
125309101 12530910 Fatigue
125309101 12530910 Memory impairment
125309101 12530910 Multiple sclerosis relapse
125309101 12530910 Muscular weakness
125309101 12530910 Urinary tract disorder
125309101 12530910 Urinary tract 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
125309101 12530910 1 20150223 0