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
119804212 11980421 2 F 201512 20160825 20160129 20160831 EXP CZ-CZSUKL-16000244 CZ-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-004232 BRISTOL MYERS SQUIBB 0.00 E F Y 0.00000 20160831 CN CZ CZ

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
119804212 11980421 1 PS ELIQUIS APIXABAN 1 Unknown U 202155
119804212 11980421 2 SS WARFARIN SODIUM. WARFARIN SODIUM 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119804212 11980421 1 Product used for unknown indication
119804212 11980421 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119804212 11980421 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
119804212 11980421 Blood blister
119804212 11980421 Contraindicated product administered
119804212 11980421 Oedema peripheral
119804212 11980421 Pain in extremity
119804212 11980421 Purpura

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
119804212 11980421 1 201512 0
119804212 11980421 2 20151027 201512 0