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
126944701 12694470 1 I 20140213 20160617 20160829 20160829 EXP US-BAYER-2016-125053 BAYER 62.00 YR A F 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
126944701 12694470 1 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK U UNKNOWN 0 20 MG FILM-COATED TABLET
126944701 12694470 2 SS XARELTO RIVAROXABAN 1 U 0 FILM-COATED TABLET
126944701 12694470 3 SS XARELTO RIVAROXABAN 1 U 0 FILM-COATED TABLET
126944701 12694470 4 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 UNK Y 999999
126944701 12694470 5 SS CLOPIDOGREL BISULFATE. CLOPIDOGREL BISULFATE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126944701 12694470 1 Thrombosis prophylaxis
126944701 12694470 2 Cerebrovascular accident prophylaxis
126944701 12694470 3 Atrial fibrillation
126944701 12694470 4 Product used for unknown indication
126944701 12694470 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126944701 12694470 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126944701 12694470 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
126944701 12694470 1 20140124 20140213 0