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
125433602 12543360 2 F 20160617 20160713 20160711 20160722 EXP GB-ALEXION PHARMACEUTICALS INC-A201604960 ALEXION 28.02 YR M Y 0.00000 20160722 CN GB GB

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
125433602 12543360 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 600 MG, QW 125166 600 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk
125433602 12543360 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W P004708 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
125433602 12543360 3 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W P0005002R 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
125433602 12543360 4 C PHENOXYMETHYLPENICILLIN PENICILLIN V 1 Unknown 500 MG, BID 0 500 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125433602 12543360 1 Paroxysmal nocturnal haemoglobinuria
125433602 12543360 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125433602 12543360 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125433602 12543360 Dyspnoea
125433602 12543360 Fatigue
125433602 12543360 Headache

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
125433602 12543360 1 20160217 20160309 0
125433602 12543360 2 20160316 0
125433602 12543360 3 20160316 0