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
124143762 12414376 2 F 20160629 20160528 20160715 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-040877 BRISTOL MYERS SQUIBB 0.00 F Y 55.00000 KG 20160715 CN 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
124143762 12414376 1 PS COUMADIN WARFARIN SODIUM 1 Oral 2.5 MG, UNK N U 9218 2.5 MG INJECTION
124143762 12414376 2 SS COUMADIN WARFARIN SODIUM 1 Oral 1 MG, UNK N U 9218 1 MG INJECTION
124143762 12414376 3 SS COUMADIN WARFARIN SODIUM 1 Oral 2 MG, QD N U 9218 2 MG INJECTION QD
124143762 12414376 4 C ESTRACE ESTRADIOL 1 Unknown 0.5 MG, QD U 0 .5 MG QD
124143762 12414376 5 C TYLENOL ACETAMINOPHEN 1 Unknown UNK, QWK U 0 /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124143762 12414376 1 Atrial fibrillation
124143762 12414376 4 Product used for unknown indication
124143762 12414376 5 Arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124143762 12414376 Asthenia
124143762 12414376 Decreased appetite
124143762 12414376 Dizziness
124143762 12414376 Feeling abnormal
124143762 12414376 International normalised ratio fluctuation
124143762 12414376 Nausea

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
124143762 12414376 3 20160427 0