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
126219311 12621931 1 I 201607 20160801 20160804 20160804 EXP US-PFIZER INC-2016370387 PFIZER 87.00 YR F Y 44.91000 KG 20160804 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
126219311 12621931 1 PS AROMASIN EXEMESTANE 1 25 MG, 1X/DAY 75 MG Y 708BH 20753 25 MG COATED TABLET QD
126219311 12621931 2 C PURINOL ALLOPURINOL 1 UP TO THREE TIMES A DAY 0
126219311 12621931 3 C PURINOL ALLOPURINOL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126219311 12621931 1 Breast cancer
126219311 12621931 2 Headache
126219311 12621931 3 Nausea

Outcome of event

Event ID CASEID OUTC COD
126219311 12621931 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126219311 12621931 Asthenia
126219311 12621931 Confusional state
126219311 12621931 Dizziness
126219311 12621931 Fatigue
126219311 12621931 Malaise
126219311 12621931 Musculoskeletal discomfort
126219311 12621931 Musculoskeletal pain
126219311 12621931 Nausea
126219311 12621931 Neck pain
126219311 12621931 Weight decreased

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
126219311 12621931 1 20160708 20160727 0