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
5483734 6616114 I 5483734-X 20071004 20071009 DIR M N 204 LBS 20071005 OT N N UNITED STATES

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
5483734 1009033692 PS PROLEUKIN 1 INTRAVENOUS 55.5 MU IV Q 8 HOURS D
5483734 1009049324 SS AVASTIN 1 INTRAVENOUS 940 MG IV Q 2 WEEKS
5483734 1009049325 C CADUET 1
5483734 1009049326 C AMBIEN 1
5483734 1009049327 C OXYCONTIN 1
5483734 1009049328 C LORTAB 1
5483734 1009049329 C ATIVAN 1
5483734 1009049331 C VICODIN 1
5483734 1009049332 C ZOLOFT 1
5483734 1009049333 C TIGAN 1

Indications of drugs used

no results found

Outcome of event

Event ID OUTC COD
5483734 HO

Reactions reported

Event ID PT
5483734 PANCREATITIS ACUTE

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
5483734 1009033692 20070927
5483734 1009049324 20070925