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
127595271 12759527 1 I 20150822 20160907 20160919 20160919 EXP CN-PFIZER INC-2016425156 PFIZER 50.00 YR F Y 58.00000 KG 20160919 OT CN CN

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
127595271 12759527 1 PS AROMASIN EXEMESTANE 1 Oral 25 MG, 1X/DAY 25 MG Y Z789P 20753 25 MG COATED TABLET QD
127595271 12759527 2 SS AROMASIN EXEMESTANE 1 Oral 25 MG, 1X/DAY 25 MG Y Z836D 20753 25 MG COATED TABLET QD
127595271 12759527 3 SS CHIDAMIDE TUCIDINOSTAT 1 Oral 30 MG, 1X/DAY 30 MG Y 20150201 0 30 MG QD
127595271 12759527 4 SS CHIDAMIDE TUCIDINOSTAT 1 Oral 30 MG, 2 TIMES EVEY 7 DAYS 30 MG Y 0 30 MG BIW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127595271 12759527 1 Breast cancer
127595271 12759527 3 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
127595271 12759527 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127595271 12759527 Abdominal distension
127595271 12759527 Abdominal pain
127595271 12759527 Nausea
127595271 12759527 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
127595271 12759527 1 20150821 20150821 0
127595271 12759527 2 20150825 20150906 0
127595271 12759527 3 20150822 20150822 0
127595271 12759527 4 20150825 20150904 0