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
124293413 12429341 3 F 20150724 20160713 20160602 20160722 EXP US-JNJFOC-20160528344 JANSSEN 55.59 YR A M 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
124293413 12429341 1 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET QD
124293413 12429341 2 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET QD
124293413 12429341 3 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET QD
124293413 12429341 4 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET QD
124293413 12429341 5 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET QD
124293413 12429341 6 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET QD
124293413 12429341 7 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET QD
124293413 12429341 8 PS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 202439 20 MG TABLET QD
124293413 12429341 9 SS IBUPROFEN. IBUPROFEN 1 Unknown U U 19012 UNSPECIFIED
124293413 12429341 10 SS IBUPROFEN. IBUPROFEN 1 Unknown 3-4 TIMES U U 19012 400 MG UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124293413 12429341 1 Thrombosis prophylaxis
124293413 12429341 2 Thrombosis prophylaxis
124293413 12429341 3 Coronary artery disease
124293413 12429341 4 Coronary artery disease
124293413 12429341 5 Atrial fibrillation
124293413 12429341 6 Atrial fibrillation
124293413 12429341 7 Cerebrovascular accident prophylaxis
124293413 12429341 8 Cerebrovascular accident prophylaxis
124293413 12429341 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124293413 12429341 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124293413 12429341 Acute kidney injury
124293413 12429341 Upper gastrointestinal 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
124293413 12429341 1 20130502 20141222 0
124293413 12429341 2 20141230 20150811 0
124293413 12429341 3 20141230 20150811 0
124293413 12429341 4 20130502 20141222 0
124293413 12429341 5 20130502 20141222 0
124293413 12429341 6 20141230 20150811 0
124293413 12429341 7 20141230 20150811 0
124293413 12429341 8 20130502 20141222 0