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
126722241 12672224 1 I 20160116 20160520 20160822 20160822 EXP US-BAYER-2016-102947 BAYER 71.00 YR E M Y 0.00000 20160822 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
126722241 12672224 1 SS XARELTO RIVAROXABAN 1 Oral 20 MG, QD 2200 MG Y N UNKNOWN 0 20 MG FILM-COATED TABLET QD
126722241 12672224 2 SS XARELTO RIVAROXABAN 1 2200 MG Y N 0 FILM-COATED TABLET
126722241 12672224 3 SS XARELTO RIVAROXABAN 1 2200 MG Y N 0 FILM-COATED TABLET
126722241 12672224 4 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 Oral 81 MG, QD Y 999999 81 MG TABLET QD
126722241 12672224 5 SS CLOPIDOGREL BISULFATE. CLOPIDOGREL BISULFATE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126722241 12672224 1 Atrial fibrillation
126722241 12672224 2 Thrombosis prophylaxis
126722241 12672224 3 Cerebrovascular accident prophylaxis
126722241 12672224 4 Product used for unknown indication
126722241 12672224 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126722241 12672224 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126722241 12672224 Acute kidney injury
126722241 12672224 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
126722241 12672224 1 20150929 20160116 0