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
123951253 12395125 3 F 201605 20160725 20160523 20160802 EXP US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-31778BP BOEHRINGER INGELHEIM 53.00 YR F Y 0.00000 20160802 MD 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
123951253 12395125 1 PS PRADAXA DABIGATRAN ETEXILATE MESYLATE 1 Oral 300 MG Y 22512 150 MG CAPSULE BID
123951253 12395125 2 SS PRADAXA DABIGATRAN ETEXILATE MESYLATE 1 Oral Y 22512 150 MG CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123951253 12395125 1 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
123951253 12395125 OT
123951253 12395125 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123951253 12395125 Cardiac perforation
123951253 12395125 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
123951253 12395125 1 201512 201605 0
123951253 12395125 2 201605 0