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
106129845 10612984 5 F 20141112 20160927 20141127 20160930 EXP PHHY2014PA151569 NOVARTIS 22.03 YR F Y 49.00000 KG 20160930 CN COUNTRY NOT SPECIFIED PA

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
106129845 10612984 1 PS GILENYA FINGOLIMOD HYDROCHLORIDE 1 Oral 0.5 MG, QD 22527 .5 MG CAPSULE QD
106129845 10612984 2 SS PREDNISOLONE. PREDNISOLONE 1 Unknown Y 0
106129845 10612984 3 SS SOLU-MEDROL METHYLPREDNISOLONE SODIUM SUCCINATE 1 Unknown U 0
106129845 10612984 4 C GRAVOL DIMENHYDRINATE 1 Endocervical U 0
106129845 10612984 5 C ACETAMINOPHEN. ACETAMINOPHEN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106129845 10612984 1 Multiple sclerosis
106129845 10612984 2 Ophthalmoplegia
106129845 10612984 3 Multiple sclerosis relapse
106129845 10612984 4 Product used for unknown indication
106129845 10612984 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
106129845 10612984 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
106129845 10612984 Abdominal discomfort
106129845 10612984 Diplegia
106129845 10612984 Gastritis
106129845 10612984 Hemiplegia
106129845 10612984 Hypoaesthesia
106129845 10612984 Influenza
106129845 10612984 Multiple sclerosis relapse
106129845 10612984 Ophthalmoplegia

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
106129845 10612984 1 20130709 0
106129845 10612984 2 20141112 20141114 0