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
111874204 11187420 4 F 20140131 20160622 20150615 20160725 PER US-JNJFOC-20150517610 JANSSEN 57.17 YR A F Y 0.00000 20160725 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
111874204 11187420 1 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET BID
111874204 11187420 2 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET QD
111874204 11187420 3 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET BID
111874204 11187420 4 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET QD
111874204 11187420 5 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET BID
111874204 11187420 6 PS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 202439 20 MG TABLET QD
111874204 11187420 7 SS IBUPROFEN. IBUPROFEN 1 Unknown U U 19012 UNSPECIFIED
111874204 11187420 8 SS IBUPROFEN. IBUPROFEN 1 Unknown U U 19012 UNSPECIFIED
111874204 11187420 9 C AMLODIPINE AMLODIPINE BESYLATE 1 Unknown 0 UNSPECIFIED
111874204 11187420 10 C SIMVASTATIN. SIMVASTATIN 1 Unknown 0 20 MG UNSPECIFIED
111874204 11187420 11 C KLOR-CON POTASSIUM CHLORIDE 1 Unknown 0 UNSPECIFIED
111874204 11187420 12 C PACERONE AMIODARONE HYDROCHLORIDE 1 Unknown 0 200 MG UNSPECIFIED
111874204 11187420 13 C HCTZ HYDROCHLOROTHIAZIDE 1 Unknown 0 UNSPECIFIED
111874204 11187420 14 C LOSARTAN. LOSARTAN 1 Unknown 0 UNSPECIFIED
111874204 11187420 15 C NIFEDIPINE. NIFEDIPINE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
111874204 11187420 1 Thrombosis prophylaxis
111874204 11187420 2 Thrombosis prophylaxis
111874204 11187420 3 Cerebrovascular accident prophylaxis
111874204 11187420 4 Cerebrovascular accident prophylaxis
111874204 11187420 5 Atrial fibrillation
111874204 11187420 6 Atrial fibrillation
111874204 11187420 8 Product used for unknown indication
111874204 11187420 9 Product used for unknown indication
111874204 11187420 10 Product used for unknown indication
111874204 11187420 11 Product used for unknown indication
111874204 11187420 12 Product used for unknown indication
111874204 11187420 13 Product used for unknown indication
111874204 11187420 14 Product used for unknown indication
111874204 11187420 15 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
111874204 11187420 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
111874204 11187420 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
111874204 11187420 1 20130808 20140131 0
111874204 11187420 2 20140715 0
111874204 11187420 3 20130808 20140131 0
111874204 11187420 4 20140715 0
111874204 11187420 5 20130808 20140131 0
111874204 11187420 6 20140715 0