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
125124882 12512488 2 F 20130312 20160824 20160630 20160902 EXP US-JNJFOC-20160512476 JANSSEN 78.20 YR E M Y 97.52000 KG 20160902 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
125124882 12512488 1 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 TABLET
125124882 12512488 2 PS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 22406 TABLET
125124882 12512488 3 SS COUMADIN WARFARIN SODIUM 1 Unknown U 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125124882 12512488 1 Deep vein thrombosis
125124882 12512488 2 Deep vein thrombosis
125124882 12512488 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125124882 12512488 HO
125124882 12512488 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125124882 12512488 Acute kidney injury
125124882 12512488 Gastrointestinal haemorrhage
125124882 12512488 Respiratory failure
125124882 12512488 Subdural haematoma

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
125124882 12512488 1 20130503 0
125124882 12512488 2 20130304 201303 0