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
125125342 12512534 2 F 20140406 20160718 20160630 20160912 PER US-JNJFOC-20160504785 JANSSEN 86.72 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
125125342 12512534 1 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 TABLET
125125342 12512534 2 PS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 22406 TABLET
125125342 12512534 3 SS IBUPROFEN. IBUPROFEN 1 Unknown U U 19012 UNSPECIFIED
125125342 12512534 4 SS IBUPROFEN. IBUPROFEN 1 Unknown U U 19012 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125125342 12512534 1 Thrombosis prophylaxis
125125342 12512534 2 Knee arthroplasty
125125342 12512534 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125125342 12512534 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125125342 12512534 Upper 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
125125342 12512534 1 201403 20140406 0
125125342 12512534 2 201403 20140406 0