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
105764634 10576463 4 F 20120420 20160822 20141111 20160830 EXP PHHY2014JP033144 NOVARTIS 46.51 YR M Y 73.00000 KG 20160830 MD JP JP

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
105764634 10576463 1 PS AFINITOR EVEROLIMUS 1 Oral 10 MG, QD 2255 MG U 22334 10 MG TABLET QD
105764634 10576463 2 SS AFINITOR EVEROLIMUS 1 Oral 5 MG, QD 2255 MG U 22334 5 MG TABLET QD
105764634 10576463 3 SS AFINITOR EVEROLIMUS 1 Oral 10 MG, QD 2255 MG U 22334 10 MG TABLET QD
105764634 10576463 4 SS AFINITOR EVEROLIMUS 1 Oral 5 MG, QD 2255 MG U 22334 5 MG TABLET QD
105764634 10576463 5 SS AFINITOR EVEROLIMUS 1 Oral 10 MG, QD 2255 MG U 22334 10 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
105764634 10576463 1 Pancreatic neuroendocrine tumour

Outcome of event

Event ID CASEID OUTC COD
105764634 10576463 OT
105764634 10576463 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
105764634 10576463 Cholangitis acute
105764634 10576463 Diarrhoea
105764634 10576463 Hepatic function abnormal
105764634 10576463 Hyperglycaemia
105764634 10576463 Malignant neoplasm progression
105764634 10576463 Metastasis
105764634 10576463 Rash

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
105764634 10576463 1 20120127 20120907 0
105764634 10576463 2 20120907 20120907 0
105764634 10576463 3 20121105 20121105 0
105764634 10576463 4 20130208 20131128 0
105764634 10576463 5 20140120 0