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
104471152 10447115 2 F 20160630 20140911 20160705 EXP PHHY2014VE112439 NOVARTIS 0.00 F Y 0.00000 20160705 CN COUNTRY NOT SPECIFIED VE

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
104471152 10447115 1 PS AFINITOR EVEROLIMUS 1 Oral 10 MG, DAILY 22334 10 MG QD
104471152 10447115 2 C AROMASIN EXEMESTANE 1 Unknown 25 MG, UNK 0 25 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
104471152 10447115 1 Breast cancer
104471152 10447115 2 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
104471152 10447115 HO
104471152 10447115 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
104471152 10447115 Aphonia
104471152 10447115 Bacterial infection
104471152 10447115 Blood glucose increased
104471152 10447115 Breast cancer
104471152 10447115 Hypersensitivity
104471152 10447115 Influenza
104471152 10447115 Nephrolithiasis
104471152 10447115 Pain
104471152 10447115 Thyroid disorder

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
104471152 10447115 1 201403 0