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
126851831 12685183 1 I 2016 20160818 20160825 20160825 EXP AT-UCBSA-2016032278 UCB 63.00 YR F Y 65.00000 KG 20160825 MD AT AT

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
126851831 12685183 1 PS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous 200 MG, EV 2 WEEKS(QOW) Y U 125160 200 MG SOLUTION FOR INJECTION QOW
126851831 12685183 2 C ORENCIA ABATACEPT 1 UNK U 0
126851831 12685183 3 C Etx ETORICOXIB 1 10 MG, WEEKLY (QW) Y U 0 10 MG /wk
126851831 12685183 4 C Aprednislon PREDNISOLONE 1 UNK U 0
126851831 12685183 5 C Aprednislon PREDNISOLONE 1 5 MG, ONCE DAILY (QD) U 0 5 MG QD
126851831 12685183 6 C Imurek AZATHIOPRINE 1 50 MG, ONCE DAILY (QD) U 0 50 MG QD
126851831 12685183 7 C SIMPONI GOLIMUMAB 1 Subcutaneous 50 MG, MONTHLY (QM) U 0 50 MG /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126851831 12685183 1 Crohn's disease
126851831 12685183 2 Product used for unknown indication
126851831 12685183 3 Product used for unknown indication
126851831 12685183 4 Product used for unknown indication
126851831 12685183 6 Product used for unknown indication
126851831 12685183 7 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126851831 12685183 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126851831 12685183 Diarrhoea haemorrhagic
126851831 12685183 Pneumonia
126851831 12685183 Synovial disorder

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
126851831 12685183 1 201602 201603 0
126851831 12685183 4 201603 2016 0
126851831 12685183 5 201607 0