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
119528222 11952822 2 F 20151207 20160825 20160125 20160831 EXP AU-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-087621 BRISTOL MYERS SQUIBB 71.50 YR M Y 0.00000 20160831 MD AU AU

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
119528222 11952822 1 PS ELIQUIS APIXABAN 1 Oral 5 MG, BID 610 MG U 202155 5 MG BID
119528222 11952822 2 SS XARELTO RIVAROXABAN 1 Unknown UNK 0
119528222 11952822 3 C RAMIPRIL. RAMIPRIL 1 Unknown U 0
119528222 11952822 4 SS PRADAXA DABIGATRAN ETEXILATE MESYLATE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119528222 11952822 1 Cerebrovascular accident prophylaxis
119528222 11952822 2 Atrial fibrillation
119528222 11952822 3 Product used for unknown indication
119528222 11952822 4 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
119528222 11952822 HO
119528222 11952822 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119528222 11952822 Contraindicated product administered
119528222 11952822 Diarrhoea
119528222 11952822 Haematochezia
119528222 11952822 Rectal haemorrhage
119528222 11952822 Rectosigmoid cancer

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
119528222 11952822 1 20150924 20151123 0
119528222 11952822 2 20151123 201511 0
119528222 11952822 4 201511 0