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
127037181 12703718 1 I 20141207 20160519 20160831 20160831 EXP US-BAYER-2016-104425 BAYER 86.00 YR E F Y 0.00000 20160831 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
127037181 12703718 1 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK Y N UNKNOWN 0 20 MG FILM-COATED TABLET
127037181 12703718 2 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK Y N UNKNOWN 0 20 MG FILM-COATED TABLET
127037181 12703718 3 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK Y N UNKNOWN 0 20 MG FILM-COATED TABLET
127037181 12703718 4 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 Unknown UNK Y 999999
127037181 12703718 5 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127037181 12703718 1 Deep vein thrombosis
127037181 12703718 2 Embolism venous
127037181 12703718 3 Deep vein thrombosis
127037181 12703718 4 Product used for unknown indication
127037181 12703718 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127037181 12703718 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127037181 12703718 Haemorrhoidal haemorrhage
127037181 12703718 Vaginal 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
127037181 12703718 1 20140722 20141207 0
127037181 12703718 2 201405 2014 0
127037181 12703718 3 201412 20141216 0