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
5117826 6139258 F 5117826-1 20060521 20060523 20060929 EXP DE-BAYER-200610682BVD BAYER PHARMACEUTICALS CORPORATION 63 YR M Y 75 KG 20060929 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
5117826 1007717854 PS VARDENAFIL 2 ORAL 21400
5117826 1007717855 C ASPIRIN 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
5117826 1007717854 ERECTILE DYSFUNCTION

Outcome of event

Event ID OUTC COD
5117826 HO

Reactions reported

Event ID PT
5117826 ALANINE AMINOTRANSFERASE INCREASED
5117826 ASPARTATE AMINOTRANSFERASE INCREASED
5117826 GLOBAL AMNESIA
5117826 HYPERTENSIVE CRISIS
5117826 MICROANGIOPATHY

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
5117826 1007717854 20060208 20060521 103 DAY
5117826 1007717855 20050524