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
125118982 12511898 2 F 201410 20160826 20160630 20160902 EXP US-JNJFOC-20160509688 JANSSEN 54.52 YR A M Y 0.00000 20160902 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
125118982 12511898 1 SS XARELTO RIVAROXABAN 1 Oral Y U UNKNOWN 0 15 MG TABLET
125118982 12511898 2 SS XARELTO RIVAROXABAN 1 Oral Y U UNKNOWN 0 15 MG TABLET
125118982 12511898 3 PS XARELTO RIVAROXABAN 1 Oral Y U UNKNOWN 202439 15 MG TABLET
125118982 12511898 4 SS ASPIRIN. ASPIRIN 1 Unknown Y 0 81 MG UNSPECIFIED
125118982 12511898 5 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown Y 0 75 MG UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125118982 12511898 1 Thrombosis prophylaxis
125118982 12511898 2 Cerebrovascular accident prophylaxis
125118982 12511898 3 Atrial fibrillation
125118982 12511898 4 Product used for unknown indication
125118982 12511898 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125118982 12511898 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125118982 12511898 Acute kidney injury
125118982 12511898 Anastomotic haemorrhage
125118982 12511898 Epistaxis

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
125118982 12511898 1 20140914 20141029 0
125118982 12511898 2 20140914 20141029 0
125118982 12511898 3 20140914 20141029 0