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
124563634 12456363 4 F 20160603 20160725 20160610 20160818 EXP PHHY2016CN079994 NOVARTIS 32.71 YR M Y 73.00000 KG 20160818 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
124563634 12456363 1 PS MYFORTIC MYCOPHENOLATE SODIUM 1 Oral 720 MG, QD 50791 720 MG QD
124563634 12456363 2 C PREDNISONE. PREDNISONE 1 Unknown 15 MG, UNK 0 15 MG
124563634 12456363 3 C TACROLIMUS. TACROLIMUS 1 Unknown 5 MG, UNK 0 5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124563634 12456363 1 Renal transplant
124563634 12456363 2 Renal transplant
124563634 12456363 3 Renal transplant

Outcome of event

Event ID CASEID OUTC COD
124563634 12456363 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124563634 12456363 Diarrhoea
124563634 12456363 Enteritis
124563634 12456363 Hydronephrosis
124563634 12456363 Ureterolithiasis

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
124563634 12456363 1 20160312 0
124563634 12456363 2 20160603 0
124563634 12456363 3 20160312 0