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
125728391 12572839 1 I 20140303 20160706 20160720 20160720 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-056349 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160720 MD US US

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
125728391 12572839 1 PS COUMADIN WARFARIN SODIUM 1 Oral 5 MG, UNK 9218 5 MG
125728391 12572839 2 SS COUMADIN WARFARIN SODIUM 1 Oral 10 MG, UNK 9218 10 MG
125728391 12572839 3 SS LOVENOX ENOXAPARIN SODIUM 1 Unknown U 0
125728391 12572839 4 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Unknown 40 MG, UNK U 0 40 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125728391 12572839 1 Thrombosis
125728391 12572839 3 Thrombosis
125728391 12572839 4 Oesophagitis

Outcome of event

Event ID CASEID OUTC COD
125728391 12572839 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125728391 12572839 Deafness
125728391 12572839 Gait disturbance
125728391 12572839 International normalised ratio increased
125728391 12572839 Malaise
125728391 12572839 Pruritus
125728391 12572839 Rash generalised
125728391 12572839 Venous thrombosis
125728391 12572839 Weight increased

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
125728391 12572839 1 201402 2014 0