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
126798341 12679834 1 I 20141117 20160210 20160824 20160824 EXP US-BAYER-2016-042885 BAYER 62.00 YR A F Y 0.00000 20160824 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
126798341 12679834 1 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK U 0 20 MG FILM-COATED TABLET
126798341 12679834 2 SS XARELTO RIVAROXABAN 1 U 0 FILM-COATED TABLET
126798341 12679834 3 SS XARELTO RIVAROXABAN 1 U 0 FILM-COATED TABLET
126798341 12679834 4 SS AGGRENOX ASPIRINDIPYRIDAMOLE 1 Unknown UNK U 0
126798341 12679834 5 PS ACETYLSALICYLIC ACID (} 100 MG, FAST RELEASE) ASPIRIN 1 Oral 81 MG, UNK U 999999 81 MG MODIFIED-RELEASE TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126798341 12679834 1 Atrial fibrillation
126798341 12679834 2 Thrombosis prophylaxis
126798341 12679834 3 Cerebrovascular accident prophylaxis
126798341 12679834 4 Product used for unknown indication
126798341 12679834 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126798341 12679834 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126798341 12679834 Haemorrhagic transformation stroke

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
126798341 12679834 1 20141112 20151106 0