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
125969341 12596934 1 I 20141222 20141230 20160727 20160727 EXP PHHY2014DE170746 NOVARTIS 63.00 YR F Y 80.00000 KG 20160727 MD 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
125969341 12596934 1 SS AFINITOR EVEROLIMUS 1 Unknown 10 MG, UNK 0 10 MG TABLET
125969341 12596934 2 SS AFINITOR EVEROLIMUS 1 Unknown 5 MG, UNK 0 5 MG TABLET
125969341 12596934 3 C EXEMESTANE. EXEMESTANE 1 Unknown 25 MG, UNK 0 25 MG
125969341 12596934 4 PS FEMARA LETROZOLE 1 Unknown UNK 20726

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125969341 12596934 1 Breast cancer
125969341 12596934 3 Product used for unknown indication
125969341 12596934 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125969341 12596934 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125969341 12596934 Alveolitis
125969341 12596934 Anaemia
125969341 12596934 Cough
125969341 12596934 Dysgeusia
125969341 12596934 Dyspnoea
125969341 12596934 Respiratory failure
125969341 12596934 Urinary tract infection

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
125969341 12596934 1 20140925 20141222 0
125969341 12596934 2 20150512 0
125969341 12596934 3 201409 20141213 0
125969341 12596934 4 20050101 20140301 0