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
126221331 12622133 1 I 20150716 20160523 20160804 20160804 EXP US-BAYER-2016-108171 BAYER 76.00 YR E M 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
126221331 12622133 1 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK U UNKNOWN 0 20 MG FILM-COATED TABLET
126221331 12622133 2 SS XARELTO RIVAROXABAN 1 U 0 FILM-COATED TABLET
126221331 12622133 3 SS XARELTO RIVAROXABAN 1 U 0 FILM-COATED TABLET
126221331 12622133 4 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 UNK Y 999999
126221331 12622133 5 SS PLAVIX CLOPIDOGREL BISULFATE 1 75 MG, UNK Y 0 75 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126221331 12622133 1 Thrombosis prophylaxis
126221331 12622133 2 Cerebrovascular accident prophylaxis
126221331 12622133 3 Atrial fibrillation
126221331 12622133 4 Product used for unknown indication
126221331 12622133 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126221331 12622133 HO
126221331 12622133 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126221331 12622133 Cerebral haemorrhage
126221331 12622133 Conjunctival haemorrhage
126221331 12622133 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
126221331 12622133 1 20130417 20150824 0