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
123443303 12344330 3 F 201407 20160822 20160507 20160912 PER US-JNJFOC-20160426424 JANSSEN 60.32 YR A 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
123443303 12344330 1 SS XARELTO RIVAROXABAN 1 Oral U UNKNOWN 0 20 MG TABLET QD
123443303 12344330 2 SS XARELTO RIVAROXABAN 1 Oral U UNKNOWN 0 20 MG TABLET
123443303 12344330 3 SS XARELTO RIVAROXABAN 1 Oral U UNKNOWN 0 20 MG TABLET
123443303 12344330 4 PS XARELTO RIVAROXABAN 1 Oral U UNKNOWN 202439 20 MG TABLET QD
123443303 12344330 5 SS ASPIRIN. ASPIRIN 1 Oral UNKNOWN 0 81 MG UNSPECIFIED QD
123443303 12344330 6 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown UNKNOWN 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123443303 12344330 1 Cerebrovascular accident prophylaxis
123443303 12344330 2 Cerebrovascular accident prophylaxis
123443303 12344330 3 Atrial fibrillation
123443303 12344330 4 Atrial fibrillation
123443303 12344330 5 Product used for unknown indication
123443303 12344330 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123443303 12344330 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123443303 12344330 Epistaxis
123443303 12344330 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
123443303 12344330 1 20140613 20140718 0
123443303 12344330 2 2014 20141120 0
123443303 12344330 3 2014 20141120 0
123443303 12344330 4 20140613 20140718 0
123443303 12344330 5 20140618 0
123443303 12344330 6 20140718 0