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
126518981 12651898 1 I 20120706 20160517 20160815 20160815 EXP US-BAYER-2016-101992 BAYER 72.00 YR E M Y 0.00000 20160815 OT 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
126518981 12651898 1 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK Y N UNKNOWN;UNKNOWN 0 20 MG FILM-COATED TABLET
126518981 12651898 2 SS XARELTO RIVAROXABAN 1 Y N 0 FILM-COATED TABLET
126518981 12651898 3 SS XARELTO RIVAROXABAN 1 Y N 0 FILM-COATED TABLET
126518981 12651898 4 PS ACETYLSALICYLIC ACID (} 100 mg) ASPIRIN 1 Unknown Y 999999
126518981 12651898 5 SS PLAVIX CLOPIDOGREL BISULFATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126518981 12651898 1 Thrombosis prophylaxis
126518981 12651898 2 Cerebrovascular accident prophylaxis
126518981 12651898 3 Atrial fibrillation
126518981 12651898 4 Product used for unknown indication
126518981 12651898 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126518981 12651898 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126518981 12651898 Haemorrhoidal haemorrhage
126518981 12651898 Retroperitoneal 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
126518981 12651898 1 20120704 20120706 0