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
112802626 11280262 6 F 20130507 20160811 20150717 20160912 PER US-JNJFOC-20150607267 JANSSEN 67.59 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
112802626 11280262 1 SS XARELTO RIVAROXABAN 1 Oral Y N 0 20 MG TABLET QD
112802626 11280262 2 SS XARELTO RIVAROXABAN 1 Oral Y N 0 20 MG TABLET QD
112802626 11280262 3 PS XARELTO RIVAROXABAN 1 Oral Y N 202439 20 MG TABLET QD
112802626 11280262 4 SS COUMADIN WARFARIN SODIUM 1 Unknown U 0 UNSPECIFIED
112802626 11280262 5 SS ASPIRIN. ASPIRIN 1 Unknown U 0 325 MG UNSPECIFIED QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112802626 11280262 1 Cerebrovascular accident prophylaxis
112802626 11280262 2 Atrial fibrillation
112802626 11280262 3 Heart rate increased
112802626 11280262 4 Product used for unknown indication
112802626 11280262 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
112802626 11280262 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
112802626 11280262 Internal haemorrhage
112802626 11280262 Pericardial 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
112802626 11280262 1 20130327 20130618 0
112802626 11280262 2 20130327 20130618 0
112802626 11280262 3 20130327 20130618 0
112802626 11280262 4 201305 201307 0