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
126649491 12664949 1 I 20151120 20160518 20160818 20160818 EXP US-BAYER-2016-102402 BAYER 67.00 YR E M Y 0.00000 20160818 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
126649491 12664949 1 SS XARELTO RIVAROXABAN 1 Oral 15 MG, QD 225 MG Y N UNKNOWN 0 15 MG FILM-COATED TABLET QD
126649491 12664949 2 SS XARELTO RIVAROXABAN 1 225 MG Y N 0 FILM-COATED TABLET
126649491 12664949 3 SS XARELTO RIVAROXABAN 1 225 MG Y N 0 FILM-COATED TABLET
126649491 12664949 4 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 Unknown UNK Y 999999
126649491 12664949 5 SS CLOPIDOGREL BISULFATE. CLOPIDOGREL BISULFATE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126649491 12664949 1 Pulmonary embolism
126649491 12664949 2 Deep vein thrombosis
126649491 12664949 3 Embolism venous
126649491 12664949 4 Catheterisation cardiac
126649491 12664949 5 Catheterisation cardiac

Outcome of event

Event ID CASEID OUTC COD
126649491 12664949 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126649491 12664949 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
126649491 12664949 1 20151106 20151120 0