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
125124342 12512434 2 F 20150308 20160727 20160630 20160912 PER US-JNJFOC-20160516635 JANSSEN 64.94 YR A F Y 63.28000 KG 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
125124342 12512434 1 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET
125124342 12512434 2 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET
125124342 12512434 3 PS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 202439 20 MG TABLET
125124342 12512434 4 SS IBUPROFEN. IBUPROFEN 1 Oral Y N 999999 TABLET
125124342 12512434 5 SS IBUPROFEN. IBUPROFEN 1 Oral Y N 0 400 MG TABLET Q8H

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125124342 12512434 1 Thrombosis prophylaxis
125124342 12512434 2 Cerebrovascular accident prophylaxis
125124342 12512434 3 Atrial fibrillation
125124342 12512434 5 Pain

Outcome of event

Event ID CASEID OUTC COD
125124342 12512434 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125124342 12512434 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
125124342 12512434 1 20120518 20150308 0
125124342 12512434 2 20120518 20150308 0
125124342 12512434 3 20120518 20150308 0