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
123848462 12384846 2 F 20151001 20160712 20160519 20160719 EXP PHEH2016US012332 NOVARTIS 0.00 F Y 0.00000 20160719 CN US US

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
123848462 12384846 1 PS AFINITOR EVEROLIMUS 1 Oral UNK UNK, QD Y 22334 TABLET QD
123848462 12384846 2 C EXEMESTANE. EXEMESTANE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123848462 12384846 1 Breast cancer
123848462 12384846 2 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
123848462 12384846 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123848462 12384846 Arthropathy
123848462 12384846 Central nervous system lesion
123848462 12384846 Fatigue
123848462 12384846 Headache
123848462 12384846 Malignant neoplasm progression
123848462 12384846 Metastases to central nervous system
123848462 12384846 Metastases to liver
123848462 12384846 Metastases to lung
123848462 12384846 Rash
123848462 12384846 Urticaria

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
123848462 12384846 1 20140901 20160701 0