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
125162263 12516226 3 F 201507 20160726 20160630 20160801 EXP US-JNJFOC-20160612945 JANSSEN 87.24 YR E F Y 0.00000 20160801 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
125162263 12516226 1 SS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 0 15 MG TABLET
125162263 12516226 2 SS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 0 15 MG TABLET
125162263 12516226 3 PS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 202439 15 MG TABLET
125162263 12516226 4 SS NORCO ACETAMINOPHENHYDROCODONE BITARTRATE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125162263 12516226 1 Atrial fibrillation
125162263 12516226 2 Thrombosis prophylaxis
125162263 12516226 3 Cerebrovascular accident prophylaxis
125162263 12516226 4 Back pain

Outcome of event

Event ID CASEID OUTC COD
125162263 12516226 DE
125162263 12516226 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125162263 12516226 Acute kidney injury
125162263 12516226 Off label use
125162263 12516226 Prescribed underdose
125162263 12516226 Sepsis
125162263 12516226 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
125162263 12516226 1 20150714 20150719 0
125162263 12516226 2 20150714 20150719 0
125162263 12516226 3 20150714 20150719 0