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
125160182 12516018 2 F 20140201 20160805 20160630 20160912 PER US-JNJFOC-20160516542 JANSSEN 92.33 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
125160182 12516018 1 SS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 0 TABLET
125160182 12516018 2 SS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 0 TABLET
125160182 12516018 3 PS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 202439 TABLET
125160182 12516018 4 SS PRADAXA DABIGATRAN ETEXILATE MESYLATE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125160182 12516018 1 Atrial fibrillation
125160182 12516018 2 Thrombosis prophylaxis
125160182 12516018 3 Cerebrovascular accident prophylaxis
125160182 12516018 4 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
125160182 12516018 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125160182 12516018 Gastrointestinal haemorrhage
125160182 12516018 Haemorrhagic anaemia

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
125160182 12516018 1 20130718 20140201 0
125160182 12516018 2 20130718 20140201 0
125160182 12516018 3 20130718 20140201 0