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
123446693 12344669 3 F 201511 20160811 20160507 20160912 PER US-JNJFOC-20160416229 JANSSEN 68.82 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
123446693 12344669 1 PS XARELTO RIVAROXABAN 1 Oral 15MG AND 20MG U U UNKNOWN 22406 15 MG TABLET
123446693 12344669 2 SS COUMADIN WARFARIN SODIUM 1 Unknown Y 0 UNSPECIFIED
123446693 12344669 3 SS COUMADIN WARFARIN SODIUM 1 Unknown Y 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123446693 12344669 1 Thrombosis
123446693 12344669 2 Pulmonary embolism
123446693 12344669 3 Deep vein thrombosis

Outcome of event

Event ID CASEID OUTC COD
123446693 12344669 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123446693 12344669 Cerebral haemorrhage
123446693 12344669 International normalised ratio increased
123446693 12344669 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
123446693 12344669 1 20150701 20151123 0
123446693 12344669 2 20151113 0
123446693 12344669 3 20151113 0