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
126003101 12600310 1 I 201509 20160520 20160727 20160727 EXP US-BAYER-2016-103288 BAYER 77.00 YR E M Y 0.00000 20160727 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
126003101 12600310 1 SS XARELTO RIVAROXABAN 1 Oral UNK N UNKNOWN 0 10 MG FILM-COATED TABLET
126003101 12600310 2 SS XARELTO RIVAROXABAN 1 N 0 FILM-COATED TABLET
126003101 12600310 3 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 Unknown UNK 999999
126003101 12600310 4 SS LOVENOX ENOXAPARIN SODIUM 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126003101 12600310 1 Thrombosis prophylaxis
126003101 12600310 2 Hip arthroplasty
126003101 12600310 3 Product used for unknown indication
126003101 12600310 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126003101 12600310 DE
126003101 12600310 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126003101 12600310 Acute respiratory failure
126003101 12600310 Cardiopulmonary failure
126003101 12600310 Coagulopathy
126003101 12600310 Colitis ischaemic
126003101 12600310 Post procedural complication
126003101 12600310 Post procedural haemorrhage
126003101 12600310 Rectal 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
126003101 12600310 1 20150912 20150921 0
126003101 12600310 4 201509 0