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
126677401 12667740 1 I 2008 20160701 20160819 20160819 EXP DE-BFARM-16221127 DE-009507513-1607DEU000822 MERCK 57.00 YR F Y 59.00000 KG 20160819 CN DE DE

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
126677401 12667740 1 PS EZETROL EZETIMIBE 1 Oral 10 MG, UNK U 21445 10 MG TABLET
126677401 12667740 2 SS INEGY 10 MG/20 MG TABLETTEN EZETIMIBESIMVASTATIN 1 UNK U 0 TABLET
126677401 12667740 3 SS ATORVASTATIN ATORVASTATIN 1 Oral DAILY DOSE: 5 MG-10 MG U 0
126677401 12667740 4 SS ROSUVASTATIN. ROSUVASTATIN 1 Oral 5 MG, UNK U 0 5 MG
126677401 12667740 5 SS CHOLESTAGEL COLESEVELAM HYDROCHLORIDE 1 Oral 625 MG, UNK U 0 625 MG
126677401 12667740 6 SS FLUVASTATIN SODIUM. FLUVASTATIN SODIUM 1 Oral 20 MG, UNK U 0 20 MG
126677401 12667740 7 C UBIQUINONES (UNSPECIFIED) 2 UNK U 0
126677401 12667740 8 C VITAMIN D CHOLECALCIFEROL 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126677401 12667740 1 Hypercholesterolaemia
126677401 12667740 2 Hypercholesterolaemia
126677401 12667740 3 Hypercholesterolaemia
126677401 12667740 4 Hypercholesterolaemia
126677401 12667740 5 Hypercholesterolaemia
126677401 12667740 6 Hypercholesterolaemia

Outcome of event

Event ID CASEID OUTC COD
126677401 12667740 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126677401 12667740 Arthralgia
126677401 12667740 Depression
126677401 12667740 Dermatitis allergic
126677401 12667740 Dry eye
126677401 12667740 Hysterectomy
126677401 12667740 Myalgia
126677401 12667740 Vascular operation

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
126677401 12667740 1 2009 0
126677401 12667740 2 2015 0
126677401 12667740 3 2008 0
126677401 12667740 4 2009 0
126677401 12667740 5 2011 0
126677401 12667740 6 2015 0
126677401 12667740 7 2008 0
126677401 12667740 8 2008 0