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
127223851 12722385 1 I 201508 20160520 20160907 20160907 EXP US-BAYER-2016-103558 BAYER 61.00 YR A M Y 0.00000 20160907 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
127223851 12722385 1 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK Y N UNKNOWN 0 20 MG FILM-COATED TABLET
127223851 12722385 2 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK Y N UNKNOWN 0 20 MG FILM-COATED TABLET
127223851 12722385 3 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK Y N UNKNOWN 0 20 MG FILM-COATED TABLET
127223851 12722385 4 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK Y N UNKNOWN 0 20 MG FILM-COATED TABLET
127223851 12722385 5 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 Oral 81 MG, QD Y 999999 81 MG TABLET QD
127223851 12722385 6 SS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 UNK Y 999999 TABLET
127223851 12722385 7 SS PLAVIX CLOPIDOGREL BISULFATE 1 75 MG, UNK 0 75 MG
127223851 12722385 8 SS PLAVIX CLOPIDOGREL BISULFATE 1 UNK 0
127223851 12722385 9 SS TICAGRELOR TICAGRELOR 1 90 MG, UNK 0 90 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127223851 12722385 1 Atrial fibrillation
127223851 12722385 2 Thrombosis prophylaxis
127223851 12722385 3 Cerebrovascular accident prophylaxis
127223851 12722385 4 Atrial fibrillation
127223851 12722385 5 Coronary arterial stent insertion
127223851 12722385 6 Coronary arterial stent insertion
127223851 12722385 7 Coronary arterial stent insertion
127223851 12722385 8 Coronary arterial stent insertion
127223851 12722385 9 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127223851 12722385 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127223851 12722385 Lower 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
127223851 12722385 1 20141021 20150125 0
127223851 12722385 2 20150727 20150926 0
127223851 12722385 3 20150311 20150610 0
127223851 12722385 4 20151001 20151007 0
127223851 12722385 5 201510 0
127223851 12722385 6 20151008 0
127223851 12722385 7 201510 0
127223851 12722385 8 20151008 0
127223851 12722385 9 201510 0