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
127543841 12754384 1 I 20160912 20160916 20160916 EXP PHJP2016JP026041 NOVARTIS 69.00 YR M Y 0.00000 20160916 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
127543841 12754384 1 PS NEORAL CYCLOSPORINE 1 Unknown 50 MG, QD 50715 50 MG CAPSULE QD
127543841 12754384 2 SS NEORAL CYCLOSPORINE 1 Unknown 200-250 MG, UNK 50715 250 MG CAPSULE QD
127543841 12754384 3 SS NEORAL CYCLOSPORINE 1 Unknown 250 MG, UNK 50715 250 MG CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127543841 12754384 1 Still's disease adult onset

Outcome of event

Event ID CASEID OUTC COD
127543841 12754384 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127543841 12754384 Alanine aminotransferase increased
127543841 12754384 Arthropathy
127543841 12754384 C-reactive protein increased
127543841 12754384 Product use issue
127543841 12754384 Pyrexia
127543841 12754384 Serum ferritin increased
127543841 12754384 Still's disease adult onset

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

no results found

Therapies reported

no results found