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
120950523 12095052 3 F 20130829 20160728 20160219 20160808 EXP US-JNJFOC-20160217434 JANSSEN 65.36 YR A M Y 0.00000 20160808 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
120950523 12095052 1 SS XARELTO RIVAROXABAN 1 Oral DOSE: 10-20 MG APPROXIMATELY, EXACT DOSAGE UNKNOWN U U 0 TABLET
120950523 12095052 2 SS XARELTO RIVAROXABAN 1 Oral DOSE: 10-20 MG APPROXIMATELY, EXACT DOSAGE UNKNOWN U U 0 TABLET
120950523 12095052 3 PS XARELTO RIVAROXABAN 1 Oral DOSE: 10-20 MG APPROXIMATELY, EXACT DOSAGE UNKNOWN U U 202439 TABLET
120950523 12095052 4 SS ASPIRIN. ASPIRIN 1 Oral U 0 81 MG TABLET QD
120950523 12095052 5 SS PLAVIX CLOPIDOGREL BISULFATE 1 Oral U 0 75 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
120950523 12095052 1 Thrombosis prophylaxis
120950523 12095052 2 Cerebrovascular accident prophylaxis
120950523 12095052 3 Atrial fibrillation
120950523 12095052 4 Product used for unknown indication
120950523 12095052 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
120950523 12095052 OT
120950523 12095052 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
120950523 12095052 Internal haemorrhage
120950523 12095052 Rectal 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
120950523 12095052 1 20120101 20150501 0
120950523 12095052 2 20120101 20150501 0
120950523 12095052 3 20120101 20150501 0