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
113413112 11341311 2 F 20130731 20160818 20150805 20160912 PER US-JNJFOC-20150721183 JANSSEN 62.76 YR A M Y 0.00000 20160912 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
113413112 11341311 1 SS XARELTO RIVAROXABAN 1 Oral N 0 20 MG TABLET
113413112 11341311 2 PS XARELTO RIVAROXABAN 1 Oral N 202439 20 MG TABLET
113413112 11341311 3 SS IBUPROFEN. IBUPROFEN 1 Unknown N 19012 UNSPECIFIED
113413112 11341311 4 SS IBUPROFEN. IBUPROFEN 1 Unknown N 19012 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
113413112 11341311 1 Cerebrovascular accident prophylaxis
113413112 11341311 2 Atrial fibrillation
113413112 11341311 4 Back pain

Outcome of event

Event ID CASEID OUTC COD
113413112 11341311 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
113413112 11341311 Increased tendency to bruise
113413112 11341311 Upper 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
113413112 11341311 1 20130607 20130731 0
113413112 11341311 2 20130607 20130731 0