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
6696495 7371461 I 6696495-3 20100222 20100414 20100421 EXP LTI2010A00048 LABORATORIES TAKEDA S.A. 68 YR M N 20100420 FRANCE

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
6696495 1013567274 PS ACTOS 1 ORAL 30 MG (30 MG, 1 IN 1 D), ORAL D D 21073
6696495 1013598254 C METFORMIN HCL 1
6696495 1013598255 C DAONIL (GLIBBNCLAMIDE) 2
6696495 1013598256 C ACARBOSE 1
6696495 1013598257 C CREATOR (ROSUVASTATIN CALCIUM) 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6696495 1013567274 TYPE 2 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6696495 OT

Reactions reported

Event ID PT
6696495 HYPERTENSION

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

Event ID RPSR COD
6696495 FGN
6696495 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6696495 1013567274 20091124 DAY