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
125163482 12516348 2 F 20150520 20160805 20160630 20160912 PER US-JNJFOC-20160618660 JANSSEN 57.98 YR A Y 104.33000 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
125163482 12516348 1 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET QD
125163482 12516348 2 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET QD
125163482 12516348 3 PS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 202439 20 MG TABLET QD
125163482 12516348 4 SS IBUPROFEN. IBUPROFEN 1 Unknown U U 19012 UNSPECIFIED
125163482 12516348 5 SS IBUPROFEN. IBUPROFEN 1 Unknown U U 19012 800 MG UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125163482 12516348 1 Atrial fibrillation
125163482 12516348 2 Thrombosis prophylaxis
125163482 12516348 3 Cerebrovascular accident prophylaxis
125163482 12516348 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125163482 12516348 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125163482 12516348 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
125163482 12516348 1 20150508 20150526 0
125163482 12516348 2 20150508 20150526 0
125163482 12516348 3 20150508 20150526 0