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
127320681 12732068 1 I 20141015 20160617 20160912 20160912 PER US-JNJFOC-20160618131 JANSSEN 79.34 YR E F Y 68.49000 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
127320681 12732068 1 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET
127320681 12732068 2 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET
127320681 12732068 3 PS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 202439 20 MG TABLET
127320681 12732068 4 SS PLAVIX CLOPIDOGREL BISULFATE 1 Oral Y 0 75 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127320681 12732068 1 Thrombosis prophylaxis
127320681 12732068 2 Cerebrovascular accident prophylaxis
127320681 12732068 3 Atrial fibrillation
127320681 12732068 4 Coronary artery disease

Outcome of event

Event ID CASEID OUTC COD
127320681 12732068 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127320681 12732068 Lower gastrointestinal 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
127320681 12732068 1 20140925 20141014 0
127320681 12732068 2 20140925 20141014 0
127320681 12732068 3 20140925 20141014 0
127320681 12732068 4 20141015 0