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
126902641 12690264 1 I 20150728 20160628 20160826 20160826 EXP US-JNJFOC-20160704537 JANSSEN 76.97 YR E F Y 0.00000 20160826 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
126902641 12690264 1 SS XARELTO RIVAROXABAN 1 Oral Y N 0 20 MG TABLET QD
126902641 12690264 2 SS XARELTO RIVAROXABAN 1 Oral Y N 0 20 MG TABLET QD
126902641 12690264 3 PS XARELTO RIVAROXABAN 1 Oral Y N 202439 20 MG TABLET QD
126902641 12690264 4 SS HEPARIN HEPARIN SODIUM 1 Unknown U 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126902641 12690264 1 Atrial fibrillation
126902641 12690264 2 Thrombosis prophylaxis
126902641 12690264 3 Cerebrovascular accident prophylaxis
126902641 12690264 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126902641 12690264 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126902641 12690264 Gastrointestinal haemorrhage
126902641 12690264 Mallory-Weiss syndrome

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
126902641 12690264 1 20150727 20150728 0
126902641 12690264 2 20150727 20150728 0
126902641 12690264 3 20150727 20150728 0