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
124954662 12495466 2 F 20140805 20160726 20160624 20160804 EXP US-BAYER-2016-123963 BAYER 87.00 YR E F Y 0.00000 20160804 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
124954662 12495466 1 SS XARELTO RIVAROXABAN 1 Oral 15 MG, UNK Y N UNKNOWN 0 15 MG FILM-COATED TABLET
124954662 12495466 2 SS XARELTO RIVAROXABAN 1 Y N 0 FILM-COATED TABLET
124954662 12495466 3 SS XARELTO RIVAROXABAN 1 Y N 0 FILM-COATED TABLET
124954662 12495466 4 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown UNK Y 0
124954662 12495466 5 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 Unknown UNK Y 999999

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124954662 12495466 1 Thrombosis prophylaxis
124954662 12495466 2 Cerebrovascular accident prophylaxis
124954662 12495466 3 Atrial fibrillation
124954662 12495466 4 Product used for unknown indication
124954662 12495466 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
124954662 12495466 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124954662 12495466 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
124954662 12495466 1 20140527 20140805 0