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
122714914 12271491 4 F 20150719 20160728 20160415 20160802 EXP PHHY2015CN089725 NOVARTIS 31.70 YR M Y 57.00000 KG 20160802 MD CN CN

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
122714914 12271491 1 PS MYFORTIC MYCOPHENOLATE SODIUM 1 Oral 1080 MG, UNK 50791 1080 MG
122714914 12271491 2 C PROGRAF TACROLIMUSTACROLIMUS ANHYDROUS 1 Unknown 5 MG, UNK U 0 5 MG
122714914 12271491 3 C PROGRAF TACROLIMUSTACROLIMUS ANHYDROUS 1 Unknown 3 MG, UNK U 0 3 MG
122714914 12271491 4 C PREDNISON PREDNISONE 1 Unknown 5 MG, UNK U 0 5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122714914 12271491 1 Renal transplant
122714914 12271491 2 Prophylaxis against transplant rejection
122714914 12271491 4 Prophylaxis against transplant rejection

Outcome of event

Event ID CASEID OUTC COD
122714914 12271491 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122714914 12271491 Chills
122714914 12271491 Liver function test abnormal
122714914 12271491 Pyrexia
122714914 12271491 Urinary tract infection

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
122714914 12271491 1 20150711 0
122714914 12271491 3 20160126 0
122714914 12271491 4 20150922 0