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
125897531 12589753 1 I 20160719 20160719 20160725 20160725 EXP FR-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-47806FF BOEHRINGER INGELHEIM 80.51 YR M Y 0.00000 20160725 PH FR FR

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
125897531 12589753 1 PS PRADAXA DABIGATRAN ETEXILATE MESYLATE 1 Oral 300 MG U 22512 150 MG CAPSULE BID
125897531 12589753 2 C TAHOR ATORVASTATIN CALCIUM 1 Unknown 20 MG 0 20 MG QD
125897531 12589753 3 C BROMAZEPAM BROMAZEPAM 1 Unknown 0
125897531 12589753 4 C LERCANIDIPINE LERCANIDIPINE 1 Unknown 20 MG 0 20 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125897531 12589753 1 Paroxysmal arrhythmia
125897531 12589753 2 Product used for unknown indication
125897531 12589753 3 Product used for unknown indication
125897531 12589753 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125897531 12589753 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125897531 12589753 Dysarthria
125897531 12589753 Hemiplegia
125897531 12589753 Ischaemic stroke

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found