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
126626371 12662637 1 I 20070515 20140428 20160818 20160818 EXP FR-ROCHE-1392151 ROCHE 0.00 M Y 0.00000 20160818 MD FR FR

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
126626371 12662637 1 PS Rituximab RITUXIMAB 1 Unknown U N 103705 1 G SOLUTION FOR INFUSION
126626371 12662637 2 SS Rituximab RITUXIMAB 1 Unknown U N 103705 1 G SOLUTION FOR INFUSION
126626371 12662637 3 SS Rituximab RITUXIMAB 1 Unknown U N 103705 1 G SOLUTION FOR INFUSION
126626371 12662637 4 SS Rituximab RITUXIMAB 1 Unknown U N 103705 1 G SOLUTION FOR INFUSION
126626371 12662637 5 SS Rituximab RITUXIMAB 1 Unknown U N 103705 500 MG SOLUTION FOR INFUSION
126626371 12662637 6 SS Rituximab RITUXIMAB 1 Unknown U N 103705 500 MG SOLUTION FOR INFUSION
126626371 12662637 7 C PARACETAMOL ACETAMINOPHEN 1 0
126626371 12662637 8 C CORTANCYL PREDNISONE 1 Unknown 0 10 MG
126626371 12662637 9 C CORTANCYL PREDNISONE 1 Unknown 0 3 MG
126626371 12662637 10 C PRAVASTATIN. PRAVASTATIN 1 Unknown 0
126626371 12662637 11 C METHOTREXATE. METHOTREXATE 1 Unknown 0 12.5 MG /wk
126626371 12662637 12 C METHOTREXATE. METHOTREXATE 1 Unknown 0
126626371 12662637 13 C METHOTREXATE. METHOTREXATE 1 Unknown 0
126626371 12662637 14 C METHYLPREDNISOLONE. METHYLPREDNISOLONE 1 Unknown 0 100 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126626371 12662637 1 Rheumatoid arthritis
126626371 12662637 7 Premedication
126626371 12662637 14 Premedication

Outcome of event

Event ID CASEID OUTC COD
126626371 12662637 DE
126626371 12662637 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126626371 12662637 Abdominal distension
126626371 12662637 Cardiac failure
126626371 12662637 Cardiogenic shock
126626371 12662637 Diabetes mellitus inadequate control
126626371 12662637 Endocarditis
126626371 12662637 Gynaecomastia
126626371 12662637 Infusion related reaction
126626371 12662637 Monoclonal gammopathy
126626371 12662637 Multiple organ dysfunction syndrome
126626371 12662637 Pneumonia
126626371 12662637 Septic shock

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
126626371 12662637 1 20070515 0
126626371 12662637 2 20070601 0
126626371 12662637 3 20090709 0
126626371 12662637 4 20090723 0
126626371 12662637 5 20110210 0
126626371 12662637 6 20110225 0
126626371 12662637 8 20070515 0
126626371 12662637 9 20090709 0
126626371 12662637 10 20070515 0
126626371 12662637 11 20090709 0
126626371 12662637 12 20110210 0
126626371 12662637 13 20110225 0