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
126158341 12615834 1 I 20150810 20160523 20160802 20160802 EXP US-BAYER-2016-106591 BAYER 79.00 YR E F Y 0.00000 20160802 OT 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
126158341 12615834 1 SS XARELTO RIVAROXABAN 1 Oral UNK 1460 MG N UNKNOWN 0 20 MG FILM-COATED TABLET QD
126158341 12615834 2 SS XARELTO RIVAROXABAN 1 1460 MG N 0 FILM-COATED TABLET
126158341 12615834 3 SS XARELTO RIVAROXABAN 1 1460 MG N 0 FILM-COATED TABLET
126158341 12615834 4 SS XARELTO RIVAROXABAN 1 1460 MG N 0 FILM-COATED TABLET
126158341 12615834 5 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 Unknown UNK 999999
126158341 12615834 6 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown UNK U 0
126158341 12615834 7 SS LOVENOX ENOXAPARIN SODIUM 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126158341 12615834 1 Cerebrovascular accident prophylaxis
126158341 12615834 2 Atrial fibrillation
126158341 12615834 3 Thrombosis
126158341 12615834 4 Embolism venous
126158341 12615834 5 Product used for unknown indication
126158341 12615834 6 Thrombosis
126158341 12615834 7 Thrombosis

Outcome of event

Event ID CASEID OUTC COD
126158341 12615834 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126158341 12615834 Gastrointestinal haemorrhage
126158341 12615834 Rectal 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
126158341 12615834 1 20150530 20150810 0