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 CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
127428071 12742807 1 I 20061031 0 20160914 20160914 DIR FDA-CTU 51.92 YR M N 130.00000 KG 20160913 N MD US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
127428071 12742807 1 PS 5-FLUOROURACIL (5-FU) FLUOROURACIL 1 0 29680 MG
127428071 12742807 2 SS BEVACIZUMAB (RHUMAB VEGF) BEVACIZUMAB 1 0 2636 MG
127428071 12742807 3 SS LEUCOVORIN CALCIUM. LEUCOVORIN CALCIUM 1 0 4240 MG
127428071 12742807 4 SS ELOXATIN OXALIPLATIN 1 0 900 MG

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
127428071 12742807 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127428071 12742807 Asthenia
127428071 12742807 Back pain
127428071 12742807 Bacterial test positive
127428071 12742807 Device deployment issue
127428071 12742807 Device related infection
127428071 12742807 Ejection fraction decreased
127428071 12742807 Hyperhidrosis
127428071 12742807 Infusion related reaction
127428071 12742807 Muscle spasms
127428071 12742807 Staphylococcus test positive
127428071 12742807 Therapy cessation
127428071 12742807 White blood cell count decreased

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127428071 12742807 1 20061010 0
127428071 12742807 2 20061010 0
127428071 12742807 3 20061010 0
127428071 12742807 4 20061010 0