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
114090013 11409001 3 F 201303 20160628 20150824 20160705 EXP CA-AMGEN-CANSP2015043431 AMGEN 87.00 YR E M Y 61.00000 KG 20160705 OT CA CA

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
114090013 11409001 1 PS ARANESP DARBEPOETIN ALFA 1 Unknown UNK U 103951 SOLUTION FOR INJECTION IN PRE-FILLED SYRINGE
114090013 11409001 2 C LIPITOR ATORVASTATIN CALCIUM 1 0
114090013 11409001 3 C VITAMIN D /00107901/ ERGOCALCIFEROL 1 0
114090013 11409001 4 C FINASTERIDE. FINASTERIDE 1 0
114090013 11409001 5 C ZYLOPRIN 2 0
114090013 11409001 6 C PREDNISONE. PREDNISONE 1 5 MG, UNK 0 5 MG
114090013 11409001 7 C ACETAMINOPHEN. ACETAMINOPHEN 1 300 MG, UNK 0 300 MG
114090013 11409001 8 C CAFFEINE. CAFFEINE 1 300 MG, UNK 0 300 MG
114090013 11409001 9 C ALLOPURINOL. ALLOPURINOL 1 100 MG, UNK 0 100 MG
114090013 11409001 10 C LINAGLIPTIN LINAGLIPTIN 1 5 MG, UNK 0 5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
114090013 11409001 1 Chronic kidney disease
114090013 11409001 2 Blood cholesterol

Outcome of event

Event ID CASEID OUTC COD
114090013 11409001 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
114090013 11409001 Anti-erythropoietin antibody positive
114090013 11409001 Aplastic anaemia
114090013 11409001 Haemoglobin abnormal
114090013 11409001 Laboratory test abnormal
114090013 11409001 Therapy non-responder

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
114090013 11409001 1 20130826 0
114090013 11409001 6 20150417 0
114090013 11409001 7 20150330 0
114090013 11409001 8 20150330 0
114090013 11409001 9 20150326 0
114090013 11409001 10 20150326 0