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
106639382 10663938 2 F 20110929 20160714 20141219 20160714 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2014-001783 BRISTOL MYERS SQUIBB 64.00 YR F Y 0.00000 20160714 OT 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
106639382 10663938 1 PS WARFARIN SODIUM. WARFARIN SODIUM 1 Unknown U 9218
106639382 10663938 2 C ASPIRIN /00002701/ ASPIRIN 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106639382 10663938 1 Embolic stroke
106639382 10663938 2 Antiplatelet therapy

Outcome of event

Event ID CASEID OUTC COD
106639382 10663938 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
106639382 10663938 Anaemia
106639382 10663938 Gastrointestinal haemorrhage

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found