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
125840551 12584055 1 I 20140723 20160719 20160722 20160722 EXP US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-47590BI BOEHRINGER INGELHEIM 0.00 Y 0.00000 20160722 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
125840551 12584055 1 PS PRADAXA DABIGATRAN ETEXILATE MESYLATE 1 Unknown 150 MG 22512 75 MG CAPSULE BID
125840551 12584055 2 SS PRADAXA DABIGATRAN ETEXILATE MESYLATE 1 Unknown 150 MG 22512 75 MG CAPSULE BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125840551 12584055 1 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
125840551 12584055 HO
125840551 12584055 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125840551 12584055 Anaemia
125840551 12584055 Cerebral haemorrhage
125840551 12584055 Gastrointestinal 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
125840551 12584055 1 20110414 20140723 0