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
126249153 12624915 3 F 20160420 20160913 20160805 20160916 EXP US-PFIZER INC-2016375850 PFIZER 68.00 YR F Y 70.00000 KG 20160916 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
126249153 12624915 1 PS AROMASIN EXEMESTANE 1 Oral 25 MG, 1X/DAY Y 20753 25 MG COATED TABLET QD
126249153 12624915 2 SS EXEMESTANE. EXEMESTANE 1 Oral 25 MG, 1X/DAY Y 0 25 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126249153 12624915 1 Breast cancer
126249153 12624915 2 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
126249153 12624915 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126249153 12624915 Abdominal discomfort
126249153 12624915 Abdominal pain
126249153 12624915 Anxiety
126249153 12624915 Arthralgia
126249153 12624915 Asthenia
126249153 12624915 Dizziness
126249153 12624915 Fatigue
126249153 12624915 Headache
126249153 12624915 Insomnia
126249153 12624915 Malaise
126249153 12624915 Vomiting

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
126249153 12624915 1 20160420 0
126249153 12624915 2 20160520 20160617 0