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
122871793 12287179 3 F 201505 20160805 20160420 20160822 EXP BR-JNJFOC-20151221089 JANSSEN 68.94 YR E F Y 0.00000 20160822 CN BR BR

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
122871793 12287179 1 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N UNKNOWN 0 LYOPHILIZED POWDER
122871793 12287179 2 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N UNKNOWN 0 200 MG LYOPHILIZED POWDER
122871793 12287179 3 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N UNKNOWN 0 180 MG LYOPHILIZED POWDER
122871793 12287179 4 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N UNKNOWN 0 200 MG LYOPHILIZED POWDER
122871793 12287179 5 PS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N UNKNOWN 103772 180 MG LYOPHILIZED POWDER
122871793 12287179 6 C MAREVAN WARFARIN SODIUM 1 Unknown 0 UNSPECIFIED
122871793 12287179 7 C METHOTREXATE. METHOTREXATE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122871793 12287179 1 Rheumatoid arthritis
122871793 12287179 2 Rheumatoid arthritis
122871793 12287179 3 Rheumatoid arthritis
122871793 12287179 4 Rheumatoid arthritis
122871793 12287179 5 Rheumatoid arthritis

Outcome of event

Event ID CASEID OUTC COD
122871793 12287179 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
122871793 12287179 Aphthous ulcer
122871793 12287179 Arthralgia
122871793 12287179 Cardiac operation
122871793 12287179 Colitis
122871793 12287179 Drug ineffective
122871793 12287179 Hand deformity
122871793 12287179 Infusion related reaction
122871793 12287179 Medication residue present
122871793 12287179 Memory impairment
122871793 12287179 Neck mass
122871793 12287179 Off label use
122871793 12287179 Pain
122871793 12287179 Pain in extremity
122871793 12287179 Product use issue
122871793 12287179 Tongue discolouration
122871793 12287179 Urinary tract infection
122871793 12287179 Urticaria

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
122871793 12287179 3 20151120 0
122871793 12287179 4 20160715 0
122871793 12287179 5 201505 0