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
6690527 7348890 F 6690527-4 20100322 20100416 20100421 EXP JP-MERCK-1004USA00546 MERCK HUMAN HEALTH DIVISION 78 YR M Y 20100421 MD 20100301 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
6690527 1013542068 PS JANUVIA 1 ORAL
6690527 1013542069 SS AMARYL 1 ORAL
6690527 1013542070 SS AMARYL 1 ORAL
6690527 1013542071 SS ACTOS 1 ORAL
6690527 1013542072 C LEUPROLIDE ACETATE 2 SUBCUTANEOUS

Indications of drugs used

Event ID DRUG SEQ INDI PT
6690527 1013542068 DIABETES MELLITUS
6690527 1013542069 DIABETES MELLITUS
6690527 1013542071 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6690527 DE
6690527 HO

Reactions reported

Event ID PT
6690527 HYPOGLYCAEMIA
6690527 PNEUMONIA

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
6690527 1013542068 20100106 20100322 76 DAY
6690527 1013542069 20091125 20100322 118 DAY
6690527 1013542070 20061017 20091124 1135 DAY
6690527 1013542071 20051001 20100322
6690527 1013542072 20100301