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
118343272 11834327 2 F 20131213 20160801 20151214 20160912 PER US-JNJFOC-20151201109 JANSSEN 61.71 YR A 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
118343272 11834327 1 SS XARELTO RIVAROXABAN 1 Oral U U 0 20 MG TABLET
118343272 11834327 2 PS XARELTO RIVAROXABAN 1 Oral U U 202439 20 MG TABLET
118343272 11834327 3 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown U 0 UNSPECIFIED
118343272 11834327 4 SS LOVENOX ENOXAPARIN SODIUM 1 Unknown U 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118343272 11834327 1 Cerebrovascular accident prophylaxis
118343272 11834327 2 Atrial fibrillation
118343272 11834327 3 Product used for unknown indication
118343272 11834327 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
118343272 11834327 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
118343272 11834327 Upper gastrointestinal haemorrhage
118343272 11834327 Wound 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
118343272 11834327 1 20131120 20131221 0
118343272 11834327 2 20131120 20131221 0