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
126411291 12641129 1 I 20141104 20160506 20160810 20160810 EXP US-BAYER-2016-093397 BAYER 74.00 YR E M Y 0.00000 20160810 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
126411291 12641129 1 SS XARELTO RIVAROXABAN 1 Oral UNK U UNKNOWN 0 20 MG FILM-COATED TABLET
126411291 12641129 2 SS XARELTO RIVAROXABAN 1 U 0 FILM-COATED TABLET
126411291 12641129 3 SS XARELTO RIVAROXABAN 1 U 0 FILM-COATED TABLET
126411291 12641129 4 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 Unknown UNK Y 999999
126411291 12641129 5 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown UNK Y 0
126411291 12641129 6 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown UNK Y 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126411291 12641129 1 Atrial fibrillation
126411291 12641129 2 Thrombosis prophylaxis
126411291 12641129 3 Cerebrovascular accident prophylaxis
126411291 12641129 4 Product used for unknown indication
126411291 12641129 5 Atrial fibrillation
126411291 12641129 6 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
126411291 12641129 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126411291 12641129 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
126411291 12641129 1 20141017 20141104 0
126411291 12641129 5 201411 0
126411291 12641129 6 201411 0