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
126594481 12659448 1 I 201509 20160519 20160817 20160817 EXP US-BAYER-2016-103123 BAYER 70.00 YR E M Y 0.00000 20160817 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
126594481 12659448 1 SS XARELTO RIVAROXABAN 1 Oral 20 MG, QD U UNKNOWN 0 20 MG FILM-COATED TABLET QD
126594481 12659448 2 SS XARELTO RIVAROXABAN 1 U 0 FILM-COATED TABLET
126594481 12659448 3 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 Oral 81 MG, UNK U 999999 81 MG COATED TABLET
126594481 12659448 4 SS PLETAL CILOSTAZOL 1 Oral 100 MG, BID 0 100 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126594481 12659448 1 Peripheral arterial occlusive disease
126594481 12659448 2 Anticoagulant therapy
126594481 12659448 3 Peripheral arterial occlusive disease
126594481 12659448 4 Peripheral arterial occlusive disease

Outcome of event

Event ID CASEID OUTC COD
126594481 12659448 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126594481 12659448 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
126594481 12659448 1 20150827 20150907 0