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
100456912 10045691 2 F 20131002 20160725 20140328 20160802 EXP US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2014-BI-12886BP BOEHRINGER INGELHEIM 68.05 YR M Y 0.00000 20160802 CN 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
100456912 10045691 1 PS PRADAXA DABIGATRAN ETEXILATE MESYLATE 1 Unknown 300 MG 22512 150 MG CAPSULE BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100456912 10045691 1 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
100456912 10045691 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
100456912 10045691 Coagulopathy
100456912 10045691 Gastrointestinal ulcer haemorrhage
100456912 10045691 Haemorrhage

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
100456912 10045691 1 20101122 20131002 0