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
126293071 12629307 1 I 20160718 20160807 20160808 20160808 EXP IQ-ROCHE-1809971 ROCHE 40.00 YR M Y 95.00000 KG 20160808 MD IQ IQ

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
126293071 12629307 1 PS CELLCEPT MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL HYDROCHLORIDE 1 Oral Y M3546B01 50722 500 MG
126293071 12629307 2 SS NEORAL CYCLOSPORINE 1 Oral Y 0 100 MG
126293071 12629307 3 C PREDNISOLONE. PREDNISOLONE 1 Oral 0 5 MG
126293071 12629307 4 C DILTIAZEM. DILTIAZEM 1 Oral 0 90 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126293071 12629307 1 Renal transplant
126293071 12629307 2 Renal transplant
126293071 12629307 3 Renal transplant
126293071 12629307 4 Renal transplant

Outcome of event

Event ID CASEID OUTC COD
126293071 12629307 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126293071 12629307 Blood creatinine increased
126293071 12629307 Blood urea increased
126293071 12629307 Transplant rejection

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
126293071 12629307 1 20150107 20160725 0
126293071 12629307 2 20150107 20160725 0