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
124263083 12426308 3 F 20150706 20160729 20160601 20160804 EXP US-JNJFOC-20160528013 JANSSEN 60.14 YR A M Y 0.00000 20160804 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
124263083 12426308 1 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET
124263083 12426308 2 PS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 22406 20 MG TABLET
124263083 12426308 3 SS COUMADIN WARFARIN SODIUM 1 Oral U 0 2 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124263083 12426308 1 Pulmonary embolism
124263083 12426308 2 Deep vein thrombosis
124263083 12426308 3 Pulmonary embolism

Outcome of event

Event ID CASEID OUTC COD
124263083 12426308 OT
124263083 12426308 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124263083 12426308 Amnesia
124263083 12426308 Fall
124263083 12426308 Respiratory failure
124263083 12426308 Subarachnoid haemorrhage
124263083 12426308 Vitreous 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
124263083 12426308 1 20130307 201507 0
124263083 12426308 2 20130307 201507 0