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
90110993 9011099 3 F 20130103 20160816 20130109 20160830 EXP AR-BRISTOL-MYERS SQUIBB COMPANY-17267709 BRISTOL MYERS SQUIBB 65.01 YR M Y 96.00000 KG 20160830 OT AR AR

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
90110993 9011099 1 PS NULOJIX BELATACEPT 1 Unknown ON 17JAN13 480MG Y 125288 10 MG/KG SOLUTION FOR INFUSION
90110993 9011099 2 SS MYFORTIC MYCOPHENOLATE SODIUM 1 Unknown 720 MG, INTERMITTENT U 0 720 MG
90110993 9011099 3 SS BASILIXIMAB BASILIXIMAB 1 Unknown U 0
90110993 9011099 4 SS MEPREDNISONE MEPREDNISONE 1 Unknown UNK U 0
90110993 9011099 5 C VALGANCICLOVIR. VALGANCICLOVIR 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
90110993 9011099 1 Renal transplant
90110993 9011099 2 Renal transplant
90110993 9011099 3 Renal transplant
90110993 9011099 4 Renal transplant
90110993 9011099 5 Prophylaxis

Outcome of event

Event ID CASEID OUTC COD
90110993 9011099 HO
90110993 9011099 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
90110993 9011099 Gastroenteritis
90110993 9011099 Guillain-Barre syndrome
90110993 9011099 Overdose
90110993 9011099 Plasmapheresis
90110993 9011099 Sepsis
90110993 9011099 Transplant rejection
90110993 9011099 Urinary tract infection

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

no results found

Therapies reported

no results found