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
126677471 12667747 1 I 20160708 20160819 20160819 EXP PHHY2016BR097161 NOVARTIS 0.00 M Y 70.00000 KG 20160819 CN COUNTRY NOT SPECIFIED 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
126677471 12667747 1 PS EXELON PATCH RIVASTIGMINE 1 Transdermal (PATCH 10 CM2) Y U 674210 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM QD
126677471 12667747 2 SS EXELON PATCH RIVASTIGMINE 1 Transdermal (PATCH 10 CM2) Y U 604210 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM QD
126677471 12667747 3 SS EXELON PATCH RIVASTIGMINE 1 Transdermal (PATCH 10 CM2) Y U 022017 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM QD
126677471 12667747 4 SS EXELON PATCH RIVASTIGMINE 1 Transdermal (PATCH 10 CM2) Y U 032015 22083 9.5 MG TRANS-THERAPEUTIC-SYSTEM QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126677471 12667747 1 Apathy
126677471 12667747 2 Dementia Alzheimer's type
126677471 12667747 3 Depression

Outcome of event

Event ID CASEID OUTC COD
126677471 12667747 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126677471 12667747 Application site erythema
126677471 12667747 Application site hypersensitivity
126677471 12667747 Application site vesicles
126677471 12667747 Blister rupture
126677471 12667747 Product use issue

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

no results found

Therapies reported

no results found