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
6523913 7133271 F 6523913-3 20080101 20091229 20091231 EXP US-BAXTER-2009BH014323 BAXTER 52 YR F Y 53 KG 20091231 OT 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
6523913 1012888031 PS VANCOMYCIN HCL 1 INTRAVENOUS UNKNOWN
6523913 1012888032 SS MEROPENEM 1 INTRAVENOUS UNKNOWN
6523913 1012888033 C PAIN MEDICATION 2 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
6523913 1012888031 OSTEOMYELITIS
6523913 1012888032 OSTEOMYELITIS
6523913 1012888033 POSTOPERATIVE ANALGESIA

Outcome of event

Event ID OUTC COD
6523913 HO
6523913 OT

Reactions reported

Event ID PT
6523913 CARDIAC DISORDER
6523913 DRUG HYPERSENSITIVITY
6523913 HEART RATE ABNORMAL
6523913 MITRAL VALVE PROLAPSE

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
6523913 1012888031 20081218 20090101
6523913 1012888032 20081218 20090101
6523913 1012888033 20080101