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
114459733 11445973 3 F 20130805 20160805 20150902 20160912 PER US-JNJFOC-20150824440 JANSSEN 84.35 YR E F Y 0.00000 20160912 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
114459733 11445973 1 SS XARELTO RIVAROXABAN 1 Oral U U UNKNOWN 0 15 MG TABLET
114459733 11445973 2 SS XARELTO RIVAROXABAN 1 Oral U U UNKNOWN 0 15 MG TABLET
114459733 11445973 3 PS XARELTO RIVAROXABAN 1 Oral U U UNKNOWN 202439 15 MG TABLET
114459733 11445973 4 SS COUMADIN WARFARIN SODIUM 1 Unknown U 0 UNSPECIFIED
114459733 11445973 5 SS ASPIRIN. ASPIRIN 1 Unknown Y 0 81 MG UNSPECIFIED QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114459733 11445973 1 Atrial fibrillation
114459733 11445973 2 Embolism
114459733 11445973 3 Cerebrovascular accident prophylaxis
114459733 11445973 4 Atrial fibrillation
114459733 11445973 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
114459733 11445973 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
114459733 11445973 Gastrointestinal haemorrhage
114459733 11445973 Haematuria

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
114459733 11445973 1 20130802 201308 0
114459733 11445973 2 20130802 201308 0
114459733 11445973 3 20130802 201308 0
114459733 11445973 4 20130728 20130802 0