The Safety Rates Drug Report

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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
124374134 12437413 4 F 20160406 20160729 20160606 20160803 EXP PHHY2016DE076538 NOVARTIS 0.00 E F Y 45.00000 KG 20160803 OT DE DE

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
124374134 12437413 1 PS AFINITOR EVEROLIMUS 1 Oral 5 MG, QD 1158 MG N 22334 5 MG TABLET QD
124374134 12437413 2 SS AFINITOR EVEROLIMUS 1 Oral 10 MG, QD 1158 MG N 22334 10 MG TABLET QD
124374134 12437413 3 SS AFINITOR EVEROLIMUS 1 Oral 7.5 MG, QD 1158 MG N 22334 7.5 MG TABLET QD
124374134 12437413 4 SS AFINITOR EVEROLIMUS 1 Oral 5 MG, QD 1158 MG N 22334 5 MG TABLET QD
124374134 12437413 5 C EXEMESTANE. EXEMESTANE 1 Oral 25 MG, QD 3975 MG N 0 25 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124374134 12437413 1 Breast cancer metastatic
124374134 12437413 5 Breast cancer metastatic

Outcome of event

Event ID CASEID OUTC COD
124374134 12437413 OT
124374134 12437413 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124374134 12437413 Asthenia
124374134 12437413 Dementia
124374134 12437413 Fatigue
124374134 12437413 General physical health deterioration
124374134 12437413 Weight decreased

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
124374134 12437413 1 20151218 20160210 0
124374134 12437413 2 20160211 20160406 0
124374134 12437413 3 20160407 20160509 0
124374134 12437413 4 20160510 20160524 0
124374134 12437413 5 20151218 20160601 0