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
125146872 12514687 2 F 20141207 20160818 20160630 20160912 PER US-JNJFOC-20160524932 JANSSEN 86.40 YR E F 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
125146872 12514687 1 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET
125146872 12514687 2 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET
125146872 12514687 3 PS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 22406 20 MG TABLET
125146872 12514687 4 SS ASPIRIN. ASPIRIN 1 Unknown Y 0 UNSPECIFIED
125146872 12514687 5 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown Y 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125146872 12514687 1 Deep vein thrombosis
125146872 12514687 2 Deep vein thrombosis
125146872 12514687 3 Deep vein thrombosis
125146872 12514687 4 Product used for unknown indication
125146872 12514687 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125146872 12514687 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125146872 12514687 Haemorrhoidal haemorrhage
125146872 12514687 Vaginal 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
125146872 12514687 1 20140722 20141207 0
125146872 12514687 2 201405 2014 0
125146872 12514687 3 201412 20141216 0