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
126848701 12684870 1 I 20140921 20160603 20160825 20160825 EXP US-BAYER-2016-121063 BAYER 85.00 YR E F Y 0.00000 20160825 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
126848701 12684870 1 SS XARELTO RIVAROXABAN 1 Oral UNK N UNKNOWN 0 20 MG FILM-COATED TABLET
126848701 12684870 2 SS XARELTO RIVAROXABAN 1 N 0 FILM-COATED TABLET
126848701 12684870 3 SS XARELTO RIVAROXABAN 1 N 0 FILM-COATED TABLET
126848701 12684870 4 SS MOTRIN IBUPROFEN 1 Unknown UNK 0
126848701 12684870 5 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 UNK UNK, QD 999999 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126848701 12684870 1 Atrial fibrillation
126848701 12684870 2 Thrombosis prophylaxis
126848701 12684870 3 Cerebrovascular accident prophylaxis
126848701 12684870 4 Product used for unknown indication
126848701 12684870 5 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
126848701 12684870 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126848701 12684870 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
126848701 12684870 1 20130924 20141030 0