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
125826601 12582660 1 I 20150615 20160516 20160722 20160722 EXP US-BAYER-2016-101379 BAYER 42.00 YR A F 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
125826601 12582660 1 SS XARELTO RIVAROXABAN 1 Oral 15 MG, UNK Y N UNKNOWN 0 15 MG FILM-COATED TABLET
125826601 12582660 2 SS XARELTO RIVAROXABAN 1 Y N 0 FILM-COATED TABLET
125826601 12582660 3 SS XARELTO RIVAROXABAN 1 Y N 0 FILM-COATED TABLET
125826601 12582660 4 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 Unknown UNK Y 999999
125826601 12582660 5 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown 75 MG, QD 0 75 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125826601 12582660 1 Atrial fibrillation
125826601 12582660 2 Thrombosis prophylaxis
125826601 12582660 3 Cerebrovascular accident prophylaxis
125826601 12582660 4 Cardiac disorder
125826601 12582660 5 Cardiac disorder

Outcome of event

Event ID CASEID OUTC COD
125826601 12582660 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125826601 12582660 Coagulopathy
125826601 12582660 Intra-abdominal haematoma
125826601 12582660 Vaginal 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
125826601 12582660 1 20150614 20150627 0