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
125825423 12582542 3 F 20160819 20160722 20160824 EXP PHJP2016JP020718 NOVARTIS 39.00 YR M Y 48.00000 KG 20160824 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
125825423 12582542 1 PS NEORAL CYCLOSPORINE 1 Oral UNK 50715 CAPSULE
125825423 12582542 2 SS CERTICAN EVEROLIMUS 1 Oral UNK N 0 TABLET
125825423 12582542 3 C PREDNISOLONE. PREDNISOLONE 1 Oral UNK 0 TABLET
125825423 12582542 4 C CELLCEPT MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125825423 12582542 1 Renal transplant
125825423 12582542 2 Renal transplant
125825423 12582542 3 Renal transplant
125825423 12582542 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125825423 12582542 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125825423 12582542 Blood creatinine increased
125825423 12582542 Protein urine present
125825423 12582542 Renal artery arteriosclerosis
125825423 12582542 Renal tubular disorder

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

no results found

Therapies reported

no results found