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
126455831 12645583 1 I 20160802 20160811 20160811 EXP ES-JNJFOC-20160806595 JANSSEN LYDIA ABASOLO, ZULEMA ROSALES, DAVID DIAZ-VALLE, ALEJANDRO GOMEZ-GOMEZ, RAMYA C. PENA-BLANCO, ANGELA PRIETO-GARCIA, ET AL. IMMUNOSUPPRESSIVE DRUG DISCONTINUATION IN NONINFECTIOUS UVEITIS FROM REAL-LIFE CLINICAL PRACTICE: A SURVIVAL ANALYSIS. AMERICAN JOURNAL OF OPHTHALMOLOGY 01-SEP-2016;169:1-8. 0.00 Y 0.00000 20160811 MD ES ES

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
126455831 12645583 1 PS GOLIMUMAB GOLIMUMAB 1 Subcutaneous U 125289 SOLUTION FOR INJECTION
126455831 12645583 2 SS INFLIXIMAB, RECOMBINANT INFLIXIMAB 1 Intravenous (not otherwise specified) U 103772 LYOPHILIZED POWDER
126455831 12645583 3 SS CYCLOSPORINE. CYCLOSPORINE 1 Unknown 0 UNSPECIFIED
126455831 12645583 4 SS METHOTREXATE. METHOTREXATE 1 Unknown 0 UNSPECIFIED
126455831 12645583 5 SS AZATHIOPRINE. AZATHIOPRINE 1 Unknown 0 UNSPECIFIED
126455831 12645583 6 SS ADALIMUMAB ADALIMUMAB 1 Unknown 0 UNSPECIFIED
126455831 12645583 7 SS ETANERCEPT ETANERCEPT 1 Unknown 0 UNSPECIFIED
126455831 12645583 8 SS CYCLOPHOSPHAMIDE. CYCLOPHOSPHAMIDE 1 Unknown 0 UNSPECIFIED
126455831 12645583 9 SS MYCOPHENOLATE MYCOPHENOLIC ACID 1 Unknown 0 UNSPECIFIED
126455831 12645583 10 SS TACROLIMUS. TACROLIMUS 1 Unknown 0 UNSPECIFIED
126455831 12645583 11 SS TOCILIZUMAB TOCILIZUMAB 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126455831 12645583 1 Uveitis
126455831 12645583 2 Uveitis
126455831 12645583 3 Uveitis
126455831 12645583 4 Uveitis
126455831 12645583 5 Uveitis
126455831 12645583 6 Uveitis
126455831 12645583 7 Uveitis
126455831 12645583 8 Uveitis
126455831 12645583 9 Uveitis
126455831 12645583 10 Uveitis
126455831 12645583 11 Uveitis

Outcome of event

Event ID CASEID OUTC COD
126455831 12645583 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126455831 12645583 Adverse drug reaction
126455831 12645583 Drug ineffective for unapproved indication
126455831 12645583 Gastrointestinal disorder
126455831 12645583 Hepatic enzyme increased
126455831 12645583 Infection
126455831 12645583 Off label use
126455831 12645583 Renal impairment

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

no results found

Therapies reported

no results found