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
125120522 12512052 2 F 20141104 20160801 20160630 20160912 PER US-JNJFOC-20160509646 JANSSEN 74.41 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
125120522 12512052 1 SS XARELTO RIVAROXABAN 1 Oral U U UNKNOWN 0 20 MG TABLET
125120522 12512052 2 SS XARELTO RIVAROXABAN 1 Oral U U UNKNOWN 0 20 MG TABLET
125120522 12512052 3 PS XARELTO RIVAROXABAN 1 Oral U U UNKNOWN 202439 20 MG TABLET
125120522 12512052 4 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown Y 0 UNSPECIFIED
125120522 12512052 5 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown Y 0 UNSPECIFIED
125120522 12512052 6 SS ASPIRIN. ASPIRIN 1 Unknown Y 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125120522 12512052 1 Atrial fibrillation
125120522 12512052 2 Thrombosis prophylaxis
125120522 12512052 3 Cerebrovascular accident prophylaxis
125120522 12512052 4 Atrial fibrillation
125120522 12512052 5 Atrial fibrillation
125120522 12512052 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125120522 12512052 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125120522 12512052 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
125120522 12512052 1 20141017 20141104 0
125120522 12512052 2 20141017 20141104 0
125120522 12512052 3 20141017 20141104 0
125120522 12512052 4 201411 0
125120522 12512052 5 201411 0