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
126945391 12694539 1 I 20140322 20160520 20160829 20160829 EXP US-BAYER-2016-105153 BAYER 59.00 YR A M Y 0.00000 20160829 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
126945391 12694539 1 SS XARELTO RIVAROXABAN 1 Oral UNK U UNKNOWN 0 15 MG FILM-COATED TABLET
126945391 12694539 2 SS XARELTO RIVAROXABAN 1 U 0 FILM-COATED TABLET
126945391 12694539 3 SS XARELTO RIVAROXABAN 1 U 0 FILM-COATED TABLET
126945391 12694539 4 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 Oral 81 MG, UNK U 999999 81 MG
126945391 12694539 5 SS IBUPROFEN. IBUPROFEN 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126945391 12694539 1 Atrial fibrillation
126945391 12694539 2 Thrombosis prophylaxis
126945391 12694539 3 Cerebrovascular accident prophylaxis
126945391 12694539 4 Product used for unknown indication
126945391 12694539 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126945391 12694539 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126945391 12694539 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
126945391 12694539 1 20120523 20140322 0