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
125126772 12512677 2 F 201510 20160623 20160630 20160912 PER US-JNJFOC-20160502676 JANSSEN 84.46 YR E 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
125126772 12512677 1 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 15 MG TABLET
125126772 12512677 2 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 15 MG TABLET
125126772 12512677 3 PS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 202439 15 MG TABLET
125126772 12512677 4 SS ETODOLAC. ETODOLAC 1 Unknown Y 0 TABLETS
125126772 12512677 5 SS ETODOLAC. ETODOLAC 1 Unknown Y 0 TABLETS
125126772 12512677 6 SS ALENDRONATE ALENDRONATE SODIUM 1 Unknown U 0 TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125126772 12512677 1 Thrombosis prophylaxis
125126772 12512677 2 Cerebrovascular accident prophylaxis
125126772 12512677 3 Atrial fibrillation
125126772 12512677 4 Pain in extremity
125126772 12512677 5 Back pain
125126772 12512677 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125126772 12512677 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125126772 12512677 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
125126772 12512677 1 20140314 20151007 0
125126772 12512677 2 20140314 20151007 0
125126772 12512677 3 20140314 20151007 0
125126772 12512677 4 2015 201510 0
125126772 12512677 5 2015 201510 0
125126772 12512677 6 2015 0