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
126747741 12674774 1 I 20160816 20160817 20160822 20160822 EXP US-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-54191BI BOEHRINGER INGELHEIM 61.13 YR M Y 121.00000 KG 20160822 MD COUNTRY NOT SPECIFIED 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
126747741 12674774 1 PS WARFARIN WARFARIN 1 Oral 5 MG N 22512 5 MG CAPSULE QD
126747741 12674774 2 SS WARFARIN WARFARIN 1 N 22512
126747741 12674774 3 C ASPIRIN. ASPIRIN 1 Unknown 0
126747741 12674774 4 C PLAVIX CLOPIDOGREL BISULFATE 1 Oral 75 MG 0 75 MG QD
126747741 12674774 5 C ANGIOMAX BIVALIRUDIN 1 Other ROUTE: INFUSION; DAILY DOSE/DOSE PER APP: 93/75MG 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126747741 12674774 1 Atrial fibrillation
126747741 12674774 2 Coronary artery disease
126747741 12674774 3 Coronary artery disease
126747741 12674774 4 Coronary artery disease
126747741 12674774 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126747741 12674774 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126747741 12674774 Anaemia
126747741 12674774 Cardiac failure congestive
126747741 12674774 Dyspnoea

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
126747741 12674774 1 20160816 0
126747741 12674774 3 20160608 0
126747741 12674774 4 20160505 20160817 0
126747741 12674774 5 20160505 20160505 0