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
125255081 12525508 1 I 20130430 20150512 20160704 20160704 EXP PHHY2015KR175946 NOVARTIS 0.00 Y 0.00000 20160705 MD KR KR

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
125255081 12525508 1 PS FEMARA LETROZOLE 1 Unknown UNK 20726
125255081 12525508 2 SS AFINITOR EVEROLIMUS 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125255081 12525508 1 Product used for unknown indication
125255081 12525508 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125255081 12525508 OT
125255081 12525508 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125255081 12525508 Blood glucose increased
125255081 12525508 Death
125255081 12525508 Metastases to bone
125255081 12525508 Metastases to liver
125255081 12525508 Metastases to peritoneum
125255081 12525508 Metastases to spleen
125255081 12525508 Metastases to urinary tract

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
125255081 12525508 2 20130416 0