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
122307953 12230795 3 F 201501 20160811 20160401 20160912 PER US-JNJFOC-20160301362 JANSSEN 67.92 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
122307953 12230795 1 SS XARELTO RIVAROXABAN 1 Oral U U UNKNOWN 0 15 MG TABLET
122307953 12230795 2 SS XARELTO RIVAROXABAN 1 Oral U U UNKNOWN 0 TABLET
122307953 12230795 3 SS XARELTO RIVAROXABAN 1 Oral U U UNKNOWN 0 TABLET
122307953 12230795 4 PS XARELTO RIVAROXABAN 1 Oral U U UNKNOWN 22406 15 MG TABLET
122307953 12230795 5 SS COUMADIN WARFARIN SODIUM 1 Unknown U 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122307953 12230795 1 Thrombosis prophylaxis
122307953 12230795 2 Thrombosis prophylaxis
122307953 12230795 3 Thrombosis prophylaxis
122307953 12230795 4 Thrombosis prophylaxis
122307953 12230795 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
122307953 12230795 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122307953 12230795 Epistaxis
122307953 12230795 Haematuria
122307953 12230795 Mouth 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
122307953 12230795 1 20150330 20150429 0
122307953 12230795 2 2014 2015 0
122307953 12230795 3 2014 2015 0
122307953 12230795 4 20150330 20150429 0