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
127168071 12716807 1 I 20150724 20160520 20160906 20160906 EXP US-BAYER-2016-103603 BAYER 69.00 YR E M Y 120.80000 KG 20160906 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
127168071 12716807 1 SS XARELTO RIVAROXABAN 1 Oral UNK N UNKNOWN 0 FILM-COATED TABLET
127168071 12716807 2 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK N UNKNOWN 0 20 MG FILM-COATED TABLET
127168071 12716807 3 SS XARELTO RIVAROXABAN 1 Oral 10 MG, UNK N UNKNOWN 0 10 MG FILM-COATED TABLET
127168071 12716807 4 SS XARELTO RIVAROXABAN 1 Oral 10 MG, UNK N UNKNOWN 0 10 MG FILM-COATED TABLET
127168071 12716807 5 SS XARELTO RIVAROXABAN 1 Oral UNK N UNKNOWN 0 FILM-COATED TABLET
127168071 12716807 6 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK N UNKNOWN 0 20 MG FILM-COATED TABLET
127168071 12716807 7 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK N UNKNOWN 0 20 MG FILM-COATED TABLET
127168071 12716807 8 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK N UNKNOWN 0 20 MG FILM-COATED TABLET
127168071 12716807 9 SS XARELTO RIVAROXABAN 1 Oral UNK N UNKNOWN 0 FILM-COATED TABLET
127168071 12716807 10 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK N 0 20 MG FILM-COATED TABLET
127168071 12716807 11 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK N 0 20 MG FILM-COATED TABLET
127168071 12716807 12 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK N 0 20 MG FILM-COATED TABLET
127168071 12716807 13 SS ACETAMINOPHEN. ACETAMINOPHEN 1 Unknown UNK 0
127168071 12716807 14 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 Unknown UNK 999999

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127168071 12716807 1 Atrial fibrillation
127168071 12716807 2 Thrombosis prophylaxis
127168071 12716807 3 Cerebrovascular accident prophylaxis
127168071 12716807 4 Atrial fibrillation
127168071 12716807 5 Atrial fibrillation
127168071 12716807 6 Atrial fibrillation
127168071 12716807 7 Atrial fibrillation
127168071 12716807 8 Atrial fibrillation
127168071 12716807 9 Atrial fibrillation
127168071 12716807 10 Atrial fibrillation
127168071 12716807 11 Atrial fibrillation
127168071 12716807 12 Atrial fibrillation
127168071 12716807 13 Product used for unknown indication
127168071 12716807 14 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127168071 12716807 HO
127168071 12716807 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127168071 12716807 Gastrointestinal haemorrhage
127168071 12716807 Internal 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
127168071 12716807 1 2012 201602 0
127168071 12716807 2 20150810 0
127168071 12716807 3 20160216 20160317 0
127168071 12716807 4 20160323 20160607 0
127168071 12716807 5 20151105 0
127168071 12716807 6 20130408 20130620 0
127168071 12716807 7 20160305 0
127168071 12716807 8 20131209 20140806 0
127168071 12716807 9 20151108 0
127168071 12716807 10 20150810 0
127168071 12716807 11 20150320 0
127168071 12716807 12 20160203 0