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
80448973 8044897 3 F 20160704 20110705 20160714 EXP GB-ACCORD-009657 ACCORD MURTAZA A, ALI H, NAIR B, AHMED AK. RECURRENCE OF TUBULOINTERSTITIAL NEPHRITIS WITHOUT UVEITIS, IN A PATIENT WITH PREVIOUS TUBULOINTERSTITIAL NEPHRITIS AND UVEITIS SYNDROME AFTER TRANSPLANT. EXP CLIN TRANSPLANT. 2016 JUN 29. 20.00 YR A M Y 0.00000 20160714 OT GB GB

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
80448973 8044897 1 PS MYCOPHENOLIC ACID. MYCOPHENOLIC ACID 1 65416 300 MG/M**2 BID
80448973 8044897 2 SS TACROLIMUS. TACROLIMUS 1 U 91195
80448973 8044897 3 SS PREDNISOLONE. PREDNISOLONE 1 ALTERNATE DAY 0 10 MG
80448973 8044897 4 C METHYLPREDNISOLONE. METHYLPREDNISOLONE 1 Intravenous (not otherwise specified) 3 DOSES OF 1 G 0 1 G

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
80448973 8044897 1 Renal transplant
80448973 8044897 2 Renal transplant
80448973 8044897 3 Renal transplant

Outcome of event

Event ID CASEID OUTC COD
80448973 8044897 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
80448973 8044897 Cytomegalovirus infection
80448973 8044897 Tubulointerstitial nephritis and uveitis syndrome

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

no results found

Therapies reported

no results found