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
122307433 12230743 3 F 201108 20160805 20160401 20160912 PER US-JNJFOC-20160301282 JANSSEN 67.62 YR E M 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
122307433 12230743 1 SS XARELTO RIVAROXABAN 1 Oral U U UNKNOWN 0 TABLET
122307433 12230743 2 PS XARELTO RIVAROXABAN 1 Oral U U UNKNOWN 22406 20 MG TABLET
122307433 12230743 3 SS COUMADIN WARFARIN SODIUM 1 Oral IN VARYING DOSES OF 2.5 TO 3 AND 5 MG PER DAY. U 0 TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122307433 12230743 1 Deep vein thrombosis
122307433 12230743 2 Deep vein thrombosis
122307433 12230743 3 Thrombosis

Outcome of event

Event ID CASEID OUTC COD
122307433 12230743 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122307433 12230743 Epistaxis
122307433 12230743 Internal haemorrhage
122307433 12230743 Pre-existing disease

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
122307433 12230743 1 20110615 20110801 0
122307433 12230743 2 201211 201212 0