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
125148703 12514870 3 F 20150509 20160912 20160630 20160921 PER US-JNJFOC-20160522495 JANSSEN 63.46 YR A F Y 0.00000 20160921 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
125148703 12514870 1 SS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 0 15 MG TABLET
125148703 12514870 2 SS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 0 20 MG TABLET QD
125148703 12514870 3 SS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 0 15 MG TABLET QD
125148703 12514870 4 PS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 22406 TABLET
125148703 12514870 5 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown U 0 UNSPECIFIED
125148703 12514870 6 C TRAMADOL HYDROCHLORIDE. TRAMADOL HYDROCHLORIDE 1 Oral U 0 50 MG TABLETS QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125148703 12514870 1 Deep vein thrombosis
125148703 12514870 2 Deep vein thrombosis
125148703 12514870 3 Deep vein thrombosis
125148703 12514870 4 Deep vein thrombosis
125148703 12514870 5 Product used for unknown indication
125148703 12514870 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125148703 12514870 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125148703 12514870 Haematuria
125148703 12514870 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
125148703 12514870 1 20150505 20160526 0
125148703 12514870 2 20150527 20150605 0
125148703 12514870 3 20150610 20151014 0
125148703 12514870 4 201503 0