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
126629001 12662900 1 I 20160805 20160818 20160818 EXP IT-CIPLA LTD.-2016IT17096 CIPLA 0.00 Y 0.00000 20160818 OT IT IT

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
126629001 12662900 1 PS Irinotecan IRINOTECAN 1 180 MG/M2, 90-MINUTE U U 77219 180 MG/M**2
126629001 12662900 2 SS Cetuximab CETUXIMAB 1 Unknown 400 MG/M2, LOADING DOSE U U 0 400 MG/M**2
126629001 12662900 3 SS Cetuximab CETUXIMAB 1 250 MG/M2, WEEKLY U U 0 250 MG/M**2
126629001 12662900 4 C ATROPINE. ATROPINE 1 Unknown 0.25 MG, BEFORE EVERY INFUSION U U 0 .25 MG
126629001 12662900 5 C DEXAMETHASONE. DEXAMETHASONE 1 Unknown 20 MG, BEFORE INDUCTION COURSE U U 0 20 MG
126629001 12662900 6 C DEXAMETHASONE. DEXAMETHASONE 1 Unknown 8 MG, IN FURTHER COURSES U U 0 8 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126629001 12662900 1 Colorectal cancer metastatic
126629001 12662900 2 Colorectal cancer metastatic
126629001 12662900 4 Premedication

Outcome of event

Event ID CASEID OUTC COD
126629001 12662900 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126629001 12662900 Disease progression

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

no results found

Therapies reported

no results found