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
125559562 12555956 2 F 20140530 20160726 20160714 20160805 EXP US-BAYER-2016-130783 BAYER 70.00 YR E M Y 0.00000 20160805 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
125559562 12555956 1 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK Y N UNKNOWN 0 20 MG FILM-COATED TABLET
125559562 12555956 2 SS XARELTO RIVAROXABAN 1 Y N 0 FILM-COATED TABLET
125559562 12555956 3 SS XARELTO RIVAROXABAN 1 Y N 0 FILM-COATED TABLET
125559562 12555956 4 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown UNK N 0
125559562 12555956 5 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 Unknown UNK Y 999999 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125559562 12555956 1 Cerebrovascular accident prophylaxis
125559562 12555956 2 Thrombosis prophylaxis
125559562 12555956 3 Atrial fibrillation
125559562 12555956 4 Atrial thrombosis
125559562 12555956 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125559562 12555956 OT
125559562 12555956 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125559562 12555956 Haemoptysis
125559562 12555956 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
125559562 12555956 1 20140109 20140829 0
125559562 12555956 4 20140716 0
125559562 12555956 5 201407 0