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
125511251 12551125 1 I 20160629 20160713 20160713 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-057538 BRISTOL MYERS SQUIBB 59.00 YR M Y 0.00000 20160713 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
125511251 12551125 1 PS WARFARIN SODIUM. WARFARIN SODIUM 1 Unknown 9218
125511251 12551125 2 SS ASPIRIN. ASPIRIN 1 0
125511251 12551125 3 SS CLOPIDOGREL BISULFATE. CLOPIDOGREL BISULFATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125511251 12551125 1 Product used for unknown indication
125511251 12551125 2 Product used for unknown indication
125511251 12551125 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125511251 12551125 DE
125511251 12551125 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125511251 12551125 Gastrointestinal haemorrhage
125511251 12551125 Transfusion

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

no results found

Therapies reported

no results found