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
127595151 12759515 1 I 20160715 20160907 20160919 20160919 EXP CN-PFIZER INC-2016425195 PFIZER 53.00 YR F Y 51.00000 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
127595151 12759515 1 PS AROMASIN EXEMESTANE 1 Oral 25 MG, 1X/DAY, FROM D1 TO D28 350 MG N Z662A 20753 25 MG COATED TABLET QD
127595151 12759515 2 SS BLINDED THERAPY INVESTIGATIONAL PRODUCT 1 Oral 30 MG, 2X/WEEK (TUESDAY AND FRIDAY) 150 MG N 20150825 0 30 MG BIW
127595151 12759515 3 C OLMESARTAN OLMESARTAN 1 Oral 20 MG, DAILY 0 20 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127595151 12759515 1 Breast cancer
127595151 12759515 2 Breast cancer
127595151 12759515 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127595151 12759515 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127595151 12759515 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
127595151 12759515 1 20160702 20160720 0
127595151 12759515 2 20160702 20160715 0