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
127137951 12713795 1 I 20160826 20160904 20160904 PER US-JNJFOC-20160824674 JOHNSON AND JOHNSON 19.00 YR A M Y 0.00000 20160904 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
127137951 12713795 1 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N 474765 0 1 DF TABLET
127137951 12713795 2 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N 474765 0 2 DF TABLET
127137951 12713795 3 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N 474765 0 1 DF TABLET
127137951 12713795 4 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N 474765 0 2 DF TABLET
127137951 12713795 5 PS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N 474765 19835 1 DF TABLET
127137951 12713795 6 SS ZYRTEC CETIRIZINE HYDROCHLORIDE 1 Oral N 474765 19835 2 DF TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127137951 12713795 1 Fatigue
127137951 12713795 2 Fatigue
127137951 12713795 3 Eye pruritus
127137951 12713795 4 Eye pruritus
127137951 12713795 5 Multiple allergies
127137951 12713795 6 Multiple allergies

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127137951 12713795 Drug effect incomplete
127137951 12713795 Incorrect dose administered
127137951 12713795 Off label use
127137951 12713795 Product use issue
127137951 12713795 Therapeutic response unexpected

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found