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
125014012 12501401 2 F 20150410 20160801 20160627 20160810 EXP US-BAYER-2016-088455 BAYER 60.00 YR A M Y 0.00000 20160810 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
125014012 12501401 1 SS XARELTO RIVAROXABAN 1 Oral 10 MG, UNK Y N UNKNOWN 0 10 MG FILM-COATED TABLET
125014012 12501401 2 SS XARELTO RIVAROXABAN 1 Y N 0 FILM-COATED TABLET
125014012 12501401 3 SS XARELTO RIVAROXABAN 1 Y N 0 FILM-COATED TABLET
125014012 12501401 4 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 Unknown UNK Y 999999 TABLET
125014012 12501401 5 SS MELOXICAM. MELOXICAM 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125014012 12501401 1 Thrombosis prophylaxis
125014012 12501401 2 Hip arthroplasty
125014012 12501401 3 Embolism venous
125014012 12501401 4 Product used for unknown indication
125014012 12501401 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125014012 12501401 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125014012 12501401 Fall
125014012 12501401 Gastrointestinal 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
125014012 12501401 1 20150410 20150411 0