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
126818051 12681805 1 I 20160727 20160727 20160824 20160824 EXP PHJP2016JP021751 NOVARTIS 48.00 YR M Y 0.00000 20160824 MD JP JP

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
126818051 12681805 1 PS NEORAL CYCLOSPORINE 1 Oral 125 MG, QD 50715 125 MG CAPSULE QD
126818051 12681805 2 C PREDONINE PREDNISOLONEPREDNISOLONE ACETATEPREDNISOLONE SODIUM SUCCINATE 1 Oral 16 MG, UNK 0 16 MG TABLET
126818051 12681805 3 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Oral 20 MG, UNK 0 20 MG CAPSULE
126818051 12681805 4 C KIPRES MONTELUKAST SODIUM 1 Oral 10 MG, UNK 0 10 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126818051 12681805 1 Eosinophilic granulomatosis with polyangiitis
126818051 12681805 2 Product used for unknown indication
126818051 12681805 3 Product used for unknown indication
126818051 12681805 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126818051 12681805 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126818051 12681805 Femur fracture
126818051 12681805 Product use issue
126818051 12681805 Pyrexia

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found