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
125855162 12585516 2 F 20160311 20160809 20160725 20160822 EXP IT-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-057258 BRISTOL MYERS SQUIBB 78.03 YR M Y 0.00000 20160822 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
125855162 12585516 1 PS COUMADIN WARFARIN SODIUM 1 Oral 21.25 MG, QWK 575.989929 MG Y 9218 21.25 MG TABLET /wk
125855162 12585516 2 SS COUMADIN WARFARIN SODIUM 1 Oral 20 UNK, UNK 575.989929 MG Y 9218 20 MG TABLET /wk
125855162 12585516 3 SS NEO FURADANTIN NITROFURANTOIN 1 Oral 50 MG, QD Y 0 50 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125855162 12585516 1 Atrial fibrillation
125855162 12585516 3 Infection

Outcome of event

Event ID CASEID OUTC COD
125855162 12585516 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125855162 12585516 Epistaxis
125855162 12585516 Microcytic anaemia
125855162 12585516 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
125855162 12585516 1 20151205 20160616 0
125855162 12585516 2 20151209 20160719 0
125855162 12585516 3 20160701 20160710 0