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
125320472 12532047 2 F 20140714 20160630 20160706 20160707 EXP US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-43132BI BOEHRINGER INGELHEIM 0.00 Y 0.00000 20160707 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
125320472 12532047 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
125320472 12532047 1 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
125320472 12532047 HO
125320472 12532047 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125320472 12532047 Anaemia
125320472 12532047 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
125320472 12532047 1 20110815 20140714 0