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
120932343 12093234 3 F 201507 20160510 20160219 20160719 EXP PHHY2015FR174327 NOVARTIS 63.00 YR F Y 0.00000 20160719 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
120932343 12093234 1 PS AFINITOR EVEROLIMUS 1 Unknown 10 MG, QD Y 22334 10 MG QD
120932343 12093234 2 C EXEMESTANE. EXEMESTANE 1 Unknown 25 MG, QD U 0 25 MG QD
120932343 12093234 3 C EXEMESTANE. EXEMESTANE 1 Unknown 25 MG, QD U 0 25 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120932343 12093234 1 Breast cancer
120932343 12093234 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
120932343 12093234 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
120932343 12093234 Bone pain
120932343 12093234 Bronchial oedema
120932343 12093234 Bronchitis
120932343 12093234 Bronchospasm
120932343 12093234 Oedema peripheral
120932343 12093234 Rash
120932343 12093234 Skin oedema

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
120932343 12093234 1 20150613 20151016 0
120932343 12093234 2 20150613 20151016 0
120932343 12093234 3 20151115 0