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
123439212 12343921 2 F 201406 20160705 20160507 20160725 PER US-JNJFOC-20160409097 JANSSEN 82.40 YR E F Y 0.00000 20160725 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
123439212 12343921 1 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET
123439212 12343921 2 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET
123439212 12343921 3 PS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 202439 20 MG TABLET
123439212 12343921 4 SS IBUPROFEN. IBUPROFEN 1 Unknown U U 19012 UNSPECIFIED
123439212 12343921 5 SS IBUPROFEN. IBUPROFEN 1 Unknown U U 19012 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123439212 12343921 1 Thrombosis prophylaxis
123439212 12343921 2 Cerebrovascular accident prophylaxis
123439212 12343921 3 Atrial fibrillation
123439212 12343921 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123439212 12343921 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123439212 12343921 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
123439212 12343921 1 20120420 20140610 0
123439212 12343921 2 20120420 20140610 0
123439212 12343921 3 20120420 20140610 0