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
4869372 5953260 I 4869372-8 20051201 20051222 20051230 EXP DE-AVENTIS-200512970DE AVENTIS PHARMACEUTICALS, INC. 76 YR M Y 20051230 MD GERMANY

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
4869372 1006775824 PS LANTUS 1 21081
4869372 1006775825 SS AMARYL 1 020496
4869372 1006775826 SS CAPTOHEXAL 2
4869372 1006775827 SS ASPIRIN 1
4869372 1006775828 C METFORMIN 1

Indications of drugs used

no results found

Outcome of event

Event ID OUTC COD
4869372 OT

Reactions reported

Event ID PT
4869372 ANGIONEUROTIC OEDEMA

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

no results found

Therapies reported

no results found