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
127541071 12754107 1 I 20141031 20160902 20160916 20160916 EXP GB-AUROBINDO-AUR-APL-2016-11286 AUROBINDO 69.00 YR F Y 60.77000 KG 20160916 CN GB GB

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
127541071 12754107 1 SS Atorvastatin ATORVASTATIN 1 Oral 10MG TO 40MG N U TOO MANY TO PUT 0
127541071 12754107 2 SS PRAVASTATIN. PRAVASTATIN 1 Oral 10MG TO 40MG N U TOO MANY TO PUT 0
127541071 12754107 3 PS ROSUVASTATIN. ROSUVASTATIN 1 Oral 10MG TO 40MG N U TOO MANY TO PUT 79170
127541071 12754107 4 SS CLOFIBRATE CLOFIBRATE 1 Oral 10MG TO 40MG N U TOO MANY TO PUT 0
127541071 12754107 5 SS EZETROL EZETIMIBE 1 Oral 10MG TO 40MG N U TOO MANY TO PUT 0
127541071 12754107 6 C IBUPROFEN. IBUPROFEN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127541071 12754107 1 Blood cholesterol increased
127541071 12754107 2 Blood cholesterol increased
127541071 12754107 3 Blood cholesterol increased
127541071 12754107 4 Blood cholesterol increased
127541071 12754107 5 Blood cholesterol increased
127541071 12754107 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127541071 12754107 OT
127541071 12754107 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127541071 12754107 Arthropathy
127541071 12754107 Pain

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
127541071 12754107 1 20141019 20160819 0
127541071 12754107 2 20141019 20160819 0
127541071 12754107 3 20141019 20160819 0
127541071 12754107 4 20141019 20160819 0
127541071 12754107 5 20141019 20160819 0