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
124213943 12421394 3 F 20150901 20160623 20160531 20160707 EXP CA-JNJFOC-20160525427 JANSSEN 31.30 YR A M Y 110.00000 KG 20160707 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
124213943 12421394 1 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N FJM80012;FLM04015;FIM79011 0 1000 MG LYOPHILIZED POWDER
124213943 12421394 2 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N FJM80012;FLM04015;FIM79011 0 1000 MG LYOPHILIZED POWDER
124213943 12421394 3 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N FJM80012;FLM04015;FIM79011 0 1000 MG LYOPHILIZED POWDER
124213943 12421394 4 PS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) N FJM80012;FLM04015;FIM79011 103772 1000 MG LYOPHILIZED POWDER

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124213943 12421394 1 Colitis ulcerative
124213943 12421394 2 Colitis ulcerative
124213943 12421394 3 Colitis ulcerative
124213943 12421394 4 Colitis ulcerative

Outcome of event

Event ID CASEID OUTC COD
124213943 12421394 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124213943 12421394 Diarrhoea
124213943 12421394 Drug ineffective
124213943 12421394 General physical health deterioration
124213943 12421394 Haematochezia
124213943 12421394 Off label use
124213943 12421394 Product use issue

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
124213943 12421394 1 20151002 0
124213943 12421394 2 20150901 0
124213943 12421394 3 20160623 0
124213943 12421394 4 20160526 0