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
6770603 7407782 F 6770603-8 20100113 20100607 20100615 EXP DE-WATSON-2010-07118 WATSON YR Y 20100615 CN UNITED KINGDOM

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
6770603 1013870444 PS METFORMIN HCL 1 ORAL 500 MG, DAILY UNCONFIRMED 76818
6770603 1013870445 SS CRESTOR 1 ORAL 10 MG, DAILY
6770603 1013870446 SS JANUMET 1 ORAL 1 DF, BID (50MG SITAGLIPTIN/1000MG METFORMIN)
6770603 1013870447 SS ACTOS 1 ORAL 15 MG, DAILY
6770603 1013870448 SS OMACOR 1 ORAL 1000 MG, QID
6770603 1013870449 SS ALLOPURINOL 1 ORAL 150 MG, DAILY
6770603 1013870450 SS RASILEZ 2 ORAL 150 MG, DAILY
6770603 1013870451 C RAMIPRIL 1 ORAL 5 MG, DAILY
6770603 1013870452 C METOHEXAL SUCC 2 ORAL 47 1/2 MG, DAILY
6770603 1013870453 C SIMVAHEXAL 2 ORAL 40 MG, DAILY

Indications of drugs used

Event ID DRUG SEQ INDI PT
6770603 1013870444 TYPE 2 DIABETES MELLITUS
6770603 1013870445 HYPERLIPIDAEMIA
6770603 1013870446 TYPE 2 DIABETES MELLITUS
6770603 1013870447 TYPE 2 DIABETES MELLITUS
6770603 1013870448 HYPERTRIGLYCERIDAEMIA
6770603 1013870449 HYPERURICAEMIA
6770603 1013870450 HYPERTENSION
6770603 1013870451 HYPERTENSION
6770603 1013870452 HYPERTENSION
6770603 1013870453 HYPERLIPIDAEMIA

Outcome of event

Event ID OUTC COD
6770603 HO

Reactions reported

Event ID PT
6770603 LIVER INJURY

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
6770603 1013870444 20080701 20100422
6770603 1013870445 20091008 20100423 198 DAY
6770603 1013870446 20090710 20100423 288 DAY
6770603 1013870447 20090713 20100423 285 DAY
6770603 1013870448 20080701 20100423
6770603 1013870449 20100423
6770603 1013870450 20070101 20100423
6770603 1013870451 20051001
6770603 1013870452 20051001
6770603 1013870453 20091007