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
125958681 12595868 1 I 20140601 20160316 20160726 20160726 EXP US-BAYER-2016-058368 BAYER 80.00 YR E M Y 0.00000 20160726 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
125958681 12595868 1 SS XARELTO RIVAROXABAN 1 Oral 15 MG, UNK Y UNKNOWN 0 15 MG FILM-COATED TABLET
125958681 12595868 2 SS XARELTO RIVAROXABAN 1 Y 0 FILM-COATED TABLET
125958681 12595868 3 SS XARELTO RIVAROXABAN 1 Y 0 FILM-COATED TABLET
125958681 12595868 4 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 Unknown UNK U 999999
125958681 12595868 5 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125958681 12595868 1 Atrial fibrillation
125958681 12595868 2 Thrombosis prophylaxis
125958681 12595868 3 Cerebrovascular accident prophylaxis
125958681 12595868 4 Product used for unknown indication
125958681 12595868 5 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
125958681 12595868 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125958681 12595868 Fall
125958681 12595868 Haemorrhage
125958681 12595868 Nasal septum haematoma
125958681 12595868 Rhabdomyolysis
125958681 12595868 Soft tissue haemorrhage
125958681 12595868 Subcutaneous haematoma
125958681 12595868 Subdural haematoma

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
125958681 12595868 1 20130709 20140607 0