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
127346422 12734642 2 F 20140902 20160926 20160912 20160930 EXP US-JNJFOC-20160705720 JOHNSON AND JOHNSON 63.78 YR A F Y 0.00000 20160930 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
127346422 12734642 1 SS XARELTO RIVAROXABAN 1 Oral U U 0 20 MG TABLET
127346422 12734642 2 SS XARELTO RIVAROXABAN 1 Oral U U 0 20 MG TABLET
127346422 12734642 3 SS XARELTO RIVAROXABAN 1 Oral U U 0 20 MG TABLET
127346422 12734642 4 PS XARELTO RIVAROXABAN 1 Oral U U 202439 20 MG TABLET
127346422 12734642 5 SS MOTRIN IBUPROFEN 1 Unknown U U 19012 UNSPECIFIED
127346422 12734642 6 SS MOTRIN IBUPROFEN 1 Unknown 600 U U 19012 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127346422 12734642 1 Coronary artery disease
127346422 12734642 2 Atrial fibrillation
127346422 12734642 3 Thrombosis prophylaxis
127346422 12734642 4 Cerebrovascular accident prophylaxis
127346422 12734642 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127346422 12734642 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127346422 12734642 Gastrointestinal haemorrhage
127346422 12734642 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
127346422 12734642 1 20140514 20150301 0
127346422 12734642 2 20140514 20150301 0
127346422 12734642 3 20140514 20150301 0
127346422 12734642 4 20140514 20150301 0