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
126651451 12665145 1 I 20160811 20160818 20160818 EXP US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-066614 BRISTOL MYERS SQUIBB 0.00 Y 0.00000 20160818 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
126651451 12665145 1 PS ELIQUIS APIXABAN 1 Unknown U 202155
126651451 12665145 2 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown U 0
126651451 12665145 3 SS ASPIRIN /00002701/ ASPIRIN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126651451 12665145 1 Cerebrovascular accident prophylaxis
126651451 12665145 2 Product used for unknown indication
126651451 12665145 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126651451 12665145 HO
126651451 12665145 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126651451 12665145 Contraindicated product administered
126651451 12665145 Deep vein thrombosis

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

no results found

Therapies reported

no results found