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
119190904 11919090 4 F 201401 20160726 20160115 20160912 PER US-JNJFOC-20151225420 JANSSEN 79.18 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
119190904 11919090 1 SS XARELTO RIVAROXABAN 1 Oral BEGAN AT 15 MG INCREASED TO 20 MG Y N UNKNOWN 0 TABLET
119190904 11919090 2 PS XARELTO RIVAROXABAN 1 Oral BEGAN AT 15 MG INCREASED TO 20 MG Y N UNKNOWN 202439 TABLET
119190904 11919090 3 SS ASPIRIN. ASPIRIN 1 Unknown Y 0 325 MG UNSPECIFIED
119190904 11919090 4 SS COUMADIN WARFARIN SODIUM 1 Unknown Y 0 UNSPECIFIED
119190904 11919090 5 C AMIODARONE AMIODARONE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119190904 11919090 1 Atrial flutter
119190904 11919090 2 Cerebrovascular accident prophylaxis
119190904 11919090 3 Atrial fibrillation
119190904 11919090 4 Product used for unknown indication
119190904 11919090 5 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
119190904 11919090 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
119190904 11919090 Epistaxis
119190904 11919090 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
119190904 11919090 1 20131128 201402 0
119190904 11919090 2 20131128 201402 0
119190904 11919090 3 201402 0
119190904 11919090 4 201402 0