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
6740256 7369604 I 6740256-3 20100221 20100421 20100525 EXP JP-MERCK-1004USA03824 MERCK HUMAN HEALTH DIVISION 78 YR M Y 20100525 MD JAPAN

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
6740256 1013747498 PS JANUVIA 1 ORAL 021995
6740256 1013747499 C BUFFERIN 1 UNKNOWN
6740256 1013747500 C RENIVACE 2 UNKNOWN
6740256 1013747501 SS AMARYL 1 ORAL
6740256 1013747502 C FLUITRAN 2 UNKNOWN
6740256 1013747503 SS METFORMIN HCL 1 ORAL
6740256 1013747504 C SIGMART 2 UNKNOWN
6740256 1013747505 SS ACTOS 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6740256 1013747498 TYPE 2 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6740256 HO

Reactions reported

Event ID PT
6740256 HYPOGLYCAEMIC COMA

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
6740256 1013747498 20100212 20100221 10 DAY