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
123885733 12388573 3 F 20160718 20160520 20160811 PER US-PFIZER INC-2016235049 PFIZER 67.00 YR F Y 0.00000 20160811 OT 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
123885733 12388573 1 PS AROMASIN EXEMESTANE 1 Oral 25 MG, DAILY 20753 25 MG COATED TABLET
123885733 12388573 2 SS AROMASIN EXEMESTANE 1 Oral 25 MG, DAILY 20753 25 MG COATED TABLET
123885733 12388573 3 SS EVEROLIMUS EVEROLIMUS 1 Oral 10 MG, DAILY Y 0 10 MG TABLET
123885733 12388573 4 SS EVEROLIMUS EVEROLIMUS 1 Oral 10 MG, DAILY Y 0 10 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123885733 12388573 1 Breast cancer metastatic
123885733 12388573 2 Disease progression
123885733 12388573 3 Breast cancer metastatic
123885733 12388573 4 Disease progression

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
123885733 12388573 Diarrhoea
123885733 12388573 Hot flush

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
123885733 12388573 1 20160302 0
123885733 12388573 2 20160323 0
123885733 12388573 3 20160323 20160707 0
123885733 12388573 4 20160404 20160707 0