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
122301042 12230104 2 F 20140127 20160818 20160401 20160912 PER US-JNJFOC-20160309717 JANSSEN 80.85 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
122301042 12230104 1 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET
122301042 12230104 2 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET
122301042 12230104 3 PS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 202439 20 MG TABLET
122301042 12230104 4 SS ASPIRIN. ASPIRIN 1 Unknown Y 0 UNKNOWN
122301042 12230104 5 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown Y 0 UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122301042 12230104 1 Atrial fibrillation
122301042 12230104 2 Thrombosis prophylaxis
122301042 12230104 3 Cerebrovascular accident prophylaxis
122301042 12230104 4 Product used for unknown indication
122301042 12230104 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
122301042 12230104 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122301042 12230104 Epistaxis
122301042 12230104 Faeces discoloured
122301042 12230104 Haemorrhagic anaemia

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
122301042 12230104 1 20140117 20140127 0
122301042 12230104 2 20140117 20140127 0
122301042 12230104 3 20140117 20140127 0
122301042 12230104 4 20140127 0
122301042 12230104 5 20140127 0