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
120767485 12076748 5 F 20160131 20160829 20160215 20160901 EXP JP-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-011369 BRISTOL MYERS SQUIBB 87.00 YR M Y 0.00000 20160901 MD JP JP

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
120767485 12076748 1 PS ELIQUIS APIXABAN 1 Oral 2.5 MG, BID U 202155 2.5 MG BID
120767485 12076748 2 SS PLAVIX CLOPIDOGREL BISULFATE 1 Oral 50 MG, QD U 0 50 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120767485 12076748 1 Cerebrovascular accident prophylaxis
120767485 12076748 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
120767485 12076748 OT
120767485 12076748 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
120767485 12076748 Contraindicated product administered
120767485 12076748 Fall
120767485 12076748 Head injury
120767485 12076748 Subdural haematoma

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
120767485 12076748 1 201503 0
120767485 12076748 2 201503 0