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
126739631 12673963 1 I 20151120 20160810 20160822 20160822 EXP CN-PFIZER INC-2016389929 PFIZER 57.00 YR F Y 69.00000 KG 20160822 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
126739631 12673963 1 PS AROMASIN EXEMESTANE 1 Oral 25 MG, 1X/DAY 2350 MG Y Z789P 20753 25 MG COATED TABLET QD
126739631 12673963 2 SS AROMASIN EXEMESTANE 1 Oral 25 MG, 1X/DAY 2350 MG Y Z836D 20753 25 MG COATED TABLET QD
126739631 12673963 3 SS CHIDAMIDE TUCIDINOSTAT 1 Oral 30 MG, DAILY 810 MG Y 20150201 0 30 MG
126739631 12673963 4 SS CHIDAMIDE TUCIDINOSTAT 1 Oral 30 MG, 2X/WEEK 810 MG Y 0 30 MG BIW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126739631 12673963 1 Breast cancer
126739631 12673963 3 Breast cancer

Outcome of event

Event ID CASEID OUTC COD
126739631 12673963 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126739631 12673963 Platelet count 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
126739631 12673963 1 20150816 20150816 0
126739631 12673963 2 20150819 20151119 0
126739631 12673963 3 20150815 20150815 0
126739631 12673963 4 20150819 20151119 0