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
111383768 11138376 8 F 20150302 20160512 20150526 20160708 EXP PHHY2015FR042723 NOVARTIS 49.00 YR F Y 0.00000 20160708 MD FR FR

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
111383768 11138376 1 PS AFINITOR EVEROLIMUS 1 Oral 10 MG, QD 22334 10 MG QD
111383768 11138376 2 SS AFINITOR EVEROLIMUS 1 Oral 5 MG, QD 22334 5 MG QD
111383768 11138376 3 C EXEMESTANE. EXEMESTANE 1 Unknown 25 MG, QD 0 25 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
111383768 11138376 1 Breast cancer
111383768 11138376 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
111383768 11138376 HO
111383768 11138376 LT
111383768 11138376 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
111383768 11138376 Asthenia
111383768 11138376 Blood culture positive
111383768 11138376 Breast cancer metastatic
111383768 11138376 Device related infection
111383768 11138376 Diarrhoea
111383768 11138376 Hepatic failure
111383768 11138376 Hypocalcaemia
111383768 11138376 Hypokalaemia
111383768 11138376 Malignant neoplasm progression
111383768 11138376 Pyrexia
111383768 11138376 Sepsis
111383768 11138376 Vitamin D deficiency

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
111383768 11138376 1 20150208 20150408 0
111383768 11138376 2 20150424 20150427 0
111383768 11138376 3 20150208 0