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
126543251 12654325 1 I 20160713 20160816 20160816 EXP PHJP2016JP020263 NOVARTIS 52.00 YR F Y 0.00000 20160816 PH 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
126543251 12654325 1 PS NEORAL CYCLOSPORINE 1 Oral UNK 50715
126543251 12654325 2 C CELLCEPT MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE 1 Oral UNK N 0
126543251 12654325 3 C PREDONINE PREDNISOLONEPREDNISOLONE ACETATEPREDNISOLONE SODIUM SUCCINATE 1 Oral UNK 0
126543251 12654325 4 C CERTICAN EVEROLIMUS 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126543251 12654325 1 Renal transplant
126543251 12654325 2 Renal transplant
126543251 12654325 3 Renal transplant
126543251 12654325 4 Renal transplant

Outcome of event

Event ID CASEID OUTC COD
126543251 12654325 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126543251 12654325 Back pain
126543251 12654325 Cancer pain
126543251 12654325 Pyrexia
126543251 12654325 Renal cancer

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

no results found

Therapies reported

no results found