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
126337031 12633703 1 I 201312 20160421 20160809 20160809 EXP US-BAYER-2016-082324 BAYER 81.00 YR E F Y 0.00000 20160809 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
126337031 12633703 1 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK Y N UNKNOWN 0 20 MG FILM-COATED TABLET
126337031 12633703 2 SS XARELTO RIVAROXABAN 1 Y N 0 FILM-COATED TABLET
126337031 12633703 3 SS XARELTO RIVAROXABAN 1 Y N 0 FILM-COATED TABLET
126337031 12633703 4 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 Oral 81 MG, UNK Y N 999999 81 MG COATED TABLET
126337031 12633703 5 SS PARACETAMOL ACETAMINOPHEN 1 Oral 325 MG, UNK 0 325 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126337031 12633703 1 Thrombosis prophylaxis
126337031 12633703 2 Cerebrovascular accident prophylaxis
126337031 12633703 3 Atrial fibrillation
126337031 12633703 4 Product used for unknown indication
126337031 12633703 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126337031 12633703 HO
126337031 12633703 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126337031 12633703 Acute kidney injury
126337031 12633703 Gastrointestinal haemorrhage
126337031 12633703 International normalised ratio increased

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
126337031 12633703 1 20130421 20131203 0