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
113963695 11396369 5 F 20140624 20160816 20150819 20160825 EXP US-JNJFOC-20150805123 JANSSEN 44.85 YR A F Y 0.00000 20160825 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
113963695 11396369 1 SS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 0 20 MG TABLET
113963695 11396369 2 SS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 0 20 MG TABLET
113963695 11396369 3 SS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 0 20 MG TABLET
113963695 11396369 4 SS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 0 20 MG TABLET
113963695 11396369 5 SS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 0 20 MG TABLET
113963695 11396369 6 PS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 22406 20 MG TABLET
113963695 11396369 7 SS ASPIRIN. ASPIRIN 1 Unknown 0 UNSPECIFIED
113963695 11396369 8 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113963695 11396369 1 Cardiovascular disorder
113963695 11396369 2 Cardiovascular disorder
113963695 11396369 3 Cardiovascular disorder
113963695 11396369 4 Peripheral arterial occlusive disease
113963695 11396369 5 Peripheral arterial occlusive disease
113963695 11396369 6 Peripheral arterial occlusive disease
113963695 11396369 7 Cerebrovascular accident
113963695 11396369 8 Cerebrovascular accident

Outcome of event

Event ID CASEID OUTC COD
113963695 11396369 HO
113963695 11396369 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
113963695 11396369 Anaemia
113963695 11396369 Gastrointestinal haemorrhage
113963695 11396369 Haematemesis
113963695 11396369 Internal haemorrhage
113963695 11396369 Off label use
113963695 11396369 Product use issue
113963695 11396369 Uterine 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
113963695 11396369 1 20150831 20160227 0
113963695 11396369 2 20140807 20140906 0
113963695 11396369 3 20140624 20150515 0
113963695 11396369 4 20140807 20140906 0
113963695 11396369 5 20140624 20150515 0
113963695 11396369 6 20150831 20160227 0