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
112683673 11268367 3 F 20150214 20160721 20150714 20160912 PER US-JNJFOC-20150704912 JANSSEN 70.46 YR E M Y 166.47000 KG 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
112683673 11268367 1 SS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 0 20 MG TABLET
112683673 11268367 2 SS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 0 20 MG TABLET
112683673 11268367 3 PS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 202439 20 MG TABLET
112683673 11268367 4 SS COUMADIN WARFARIN SODIUM 1 Oral U 0 TABLET
112683673 11268367 5 SS ASPIRIN. ASPIRIN 1 Oral 0 TABLETS
112683673 11268367 6 C PROZAC FLUOXETINE HYDROCHLORIDE 1 Oral 0 20 MG CAPSULE
112683673 11268367 7 C CEFALEXIN CEPHALEXIN 1 Oral 0 CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112683673 11268367 1 Atrial fibrillation
112683673 11268367 2 Thrombosis prophylaxis
112683673 11268367 3 Cerebrovascular accident prophylaxis
112683673 11268367 4 Coagulopathy
112683673 11268367 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
112683673 11268367 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
112683673 11268367 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
112683673 11268367 1 20140524 20150227 0
112683673 11268367 2 20140524 20150227 0
112683673 11268367 3 20140524 20150227 0
112683673 11268367 4 20150427 20150630 0
112683673 11268367 5 20140524 0
112683673 11268367 7 20150524 0