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
126851671 12685167 1 I 201404 20160701 20160825 20160825 EXP US-BAYER-2016-134454 BAYER 86.00 YR E F Y 63.50000 KG 20160825 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
126851671 12685167 1 SS XARELTO RIVAROXABAN 1 Oral 15 MG, UNK N 0 15 MG FILM-COATED TABLET
126851671 12685167 2 SS XARELTO RIVAROXABAN 1 N 0 FILM-COATED TABLET
126851671 12685167 3 SS XARELTO RIVAROXABAN 1 N 0 FILM-COATED TABLET
126851671 12685167 4 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 Unknown 81 MG, UNK 999999 81 MG
126851671 12685167 5 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown 75 MG, UNK 0 75 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126851671 12685167 1 Thrombosis prophylaxis
126851671 12685167 2 Cerebrovascular accident prophylaxis
126851671 12685167 3 Atrial fibrillation
126851671 12685167 4 Product used for unknown indication
126851671 12685167 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126851671 12685167 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126851671 12685167 Epistaxis
126851671 12685167 Lower 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
126851671 12685167 1 20121212 20140416 0
126851671 12685167 4 20140416 0
126851671 12685167 5 20140416 0