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
126568351 12656835 1 I 201509 20160603 20160816 20160816 EXP US-BAYER-2016-116059 BAYER 72.00 YR E M Y 0.00000 20160816 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
126568351 12656835 1 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK UNKNOWN 0 20 MG FILM-COATED TABLET
126568351 12656835 2 SS XARELTO RIVAROXABAN 1 0 FILM-COATED TABLET
126568351 12656835 3 SS XARELTO RIVAROXABAN 1 0 FILM-COATED TABLET
126568351 12656835 4 SS TYLENOL ACETAMINOPHEN 1 0
126568351 12656835 5 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 81 MG, UNK 999999 81 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126568351 12656835 1 Thrombosis prophylaxis
126568351 12656835 2 Cerebrovascular accident prophylaxis
126568351 12656835 3 Atrial fibrillation
126568351 12656835 4 Product used for unknown indication
126568351 12656835 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126568351 12656835 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126568351 12656835 Acute kidney injury
126568351 12656835 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
126568351 12656835 1 20150709 20150924 0