The Safety Rates Drug Report

Member Login
2004.Q1    2004.Q2    2004.Q3    2004.Q4    2005.Q1    2005.Q2    2005.Q3    2005.Q4    2006.Q1    2006.Q2    2006.Q3    2006.Q4    2007.Q1    2007.Q2    2007.Q3    2007.Q4    2008.Q1    2008.Q2    2008.Q3    2008.Q4    2009.Q1    2009.Q2    2009.Q3    2009.Q4    2010.Q1    2010.Q2    2010.Q3    2010.Q4    2011.Q1    2011.Q2    2011.Q3    2011.Q4    2012.Q1    2012.Q2    2012.Q3    2012.Q4    2013.Q1    2013.Q2    2013.Q3    2013.Q4    2014.Q1    2014.Q2    2014.Q3    2014.Q4    2015.Q1    2015.Q2    2015.Q3    2015.Q4    2016.Q1    2016.Q2    2016.Q3   

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
125146602 12514660 2 F 20140908 20160811 20160630 20160912 PER US-JNJFOC-20160522731 JANSSEN 74.30 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
125146602 12514660 1 SS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 0 15 MG TABLET
125146602 12514660 2 SS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 0 15 MG TABLET
125146602 12514660 3 PS XARELTO RIVAROXABAN 1 Oral N UNKNOWN 202439 15 MG TABLET
125146602 12514660 4 SS ALEVE NAPROXEN SODIUM 1 Unknown 0 220 MG UNSPECIFIED BID
125146602 12514660 5 C LANTUS INSULIN GLARGINE 1 Unknown 0 UNSPECIFIED
125146602 12514660 6 C NOVOLOG INSULIN ASPART 1 Unknown 0 UNSPECIFIED
125146602 12514660 7 C CARDIZEM DILTIAZEM HYDROCHLORIDE 1 Unknown 0 UNSPECIFIED
125146602 12514660 8 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125146602 12514660 1 Thrombosis prophylaxis
125146602 12514660 2 Atrial fibrillation
125146602 12514660 3 Cerebrovascular accident prophylaxis
125146602 12514660 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125146602 12514660 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125146602 12514660 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
125146602 12514660 1 20140808 201410 0
125146602 12514660 2 20140808 201410 0
125146602 12514660 3 20140808 201410 0
125146602 12514660 5 1996 0
125146602 12514660 6 2002 0
125146602 12514660 7 2010 0
125146602 12514660 8 2012 0