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
125250181 12525018 1 I 20160617 20160627 20160704 20160704 EXP FR-JNJFOC-20160701082 JANSSEN 78.87 YR E M Y 0.00000 20160704 OT FR FR

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
125250181 12525018 1 SS XARELTO RIVAROXABAN 1 Oral Y N 0 20 MG TABLET QD
125250181 12525018 2 PS XARELTO RIVAROXABAN 1 Oral Y N 202439 20 MG TABLET QD
125250181 12525018 3 SS KARDEGIC ASPIRIN LYSINE 1 Unknown U 0 1 DF UNSPECIFIED QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125250181 12525018 1 Cerebrovascular accident prophylaxis
125250181 12525018 2 Atrial fibrillation
125250181 12525018 3 Arteriosclerosis

Outcome of event

Event ID CASEID OUTC COD
125250181 12525018 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125250181 12525018 Anaemia
125250181 12525018 Ecchymosis
125250181 12525018 Malaise
125250181 12525018 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
125250181 12525018 1 201602 201606 0
125250181 12525018 2 201602 201606 0
125250181 12525018 3 2015 0