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
127329661 12732966 1 I 201404 20160701 20160912 20160912 PER US-JNJFOC-20160705251 JANSSEN 86.04 YR E F Y 63.05000 KG 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
127329661 12732966 1 SS XARELTO RIVAROXABAN 1 Oral N 0 15 MG TABLET
127329661 12732966 2 SS XARELTO RIVAROXABAN 1 Oral N 0 15 MG TABLET
127329661 12732966 3 PS XARELTO RIVAROXABAN 1 Oral N 202439 15 MG TABLET
127329661 12732966 4 SS ASPIRIN. ASPIRIN 1 Unknown 0 81 MG UNSPECIFIED
127329661 12732966 5 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown 0 75 MG UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127329661 12732966 1 Thrombosis prophylaxis
127329661 12732966 2 Cerebrovascular accident prophylaxis
127329661 12732966 3 Atrial fibrillation
127329661 12732966 4 Product used for unknown indication
127329661 12732966 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127329661 12732966 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127329661 12732966 Epistaxis
127329661 12732966 Lower 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
127329661 12732966 1 20121212 20140416 0
127329661 12732966 2 20121212 20140416 0
127329661 12732966 3 20121212 20140416 0
127329661 12732966 4 20140416 0
127329661 12732966 5 20140416 0