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
126749762 12674976 2 F 20160719 20160812 20160823 20160826 EXP IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-067421 BRISTOL MYERS SQUIBB 85.78 YR F Y 0.00000 20160826 CN IT IT

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
126749762 12674976 1 PS COUMADIN WARFARIN SODIUM 1 Oral 1 U, PRN U 9218 1 DF TABLET
126749762 12674976 2 SS ASPIRIN. ASPIRIN 1 Oral 100 MG, QD 20100 MG U 0 100 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126749762 12674976 1 Atrial fibrillation
126749762 12674976 2 Thrombosis prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126749762 12674976 HO
126749762 12674976 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126749762 12674976 Anaemia
126749762 12674976 Melaena
126749762 12674976 Presyncope
126749762 12674976 Transfusion

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
126749762 12674976 1 20160101 20160719 0
126749762 12674976 2 20160101 20160719 0