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 CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6721914 7061573 F 6721914-3 20100503 20100512 EXP A0783335A GLAXOSMITHKLINE 46 YR F Y 147.7 KG 20100512 CN UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6721914 1013671409 PS AVANDIA 1 ORAL 2MG TWICE PER DAY 021071
6721914 1013671410 SS AVANDAMET 1 ORAL 1TAB TWICE PER DAY 021410

Indications of drugs used

Event ID DRUG SEQ INDI PT
6721914 1013671409 DIABETES MELLITUS
6721914 1013671410 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6721914 HO

Reactions reported

Event ID PT
6721914 ARRHYTHMIA
6721914 CEREBROVASCULAR ACCIDENT
6721914 HEADACHE
6721914 HEMIPARESIS
6721914 MYOCARDIAL INFARCTION

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6721914 1013671409 20050624 20050701
6721914 1013671410 20041209 20060701