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
126294562 12629456 2 F 201603 20160906 20160808 20160912 EXP GB-ALEXION-A201602199 ALEXION 51.38 YR M Y 0.00000 20160912 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
126294562 12629456 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK 125166 CONCENTRATE FOR SOLUTION FOR INFUSION
126294562 12629456 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, Q2W P0004102 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
126294562 12629456 3 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, Q2W P0004202 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
126294562 12629456 4 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, Q2W P0004302 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
126294562 12629456 5 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, Q2W P0004708 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
126294562 12629456 6 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, Q2W P0004801 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
126294562 12629456 7 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, UNK P0005002R 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION
126294562 12629456 8 C OXYCONTIN OXYCODONE HYDROCHLORIDE 1 Unknown 0
126294562 12629456 9 C OXYCONTIN OXYCODONE HYDROCHLORIDE 1 0
126294562 12629456 10 C PREGABALIN. PREGABALIN 1 Unknown 200 MG, TID 0 200 MG TID
126294562 12629456 11 C PENICILLIN /00000901/ PENICILLIN G 1 Unknown 0
126294562 12629456 12 C OXYNORM OXYCODONE HYDROCHLORIDE 1 Unknown UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126294562 12629456 1 Paroxysmal nocturnal haemoglobinuria
126294562 12629456 8 Abdominal pain
126294562 12629456 9 Pain
126294562 12629456 10 Product used for unknown indication
126294562 12629456 11 Product used for unknown indication
126294562 12629456 12 Abdominal pain

Outcome of event

Event ID CASEID OUTC COD
126294562 12629456 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126294562 12629456 Dyspnoea
126294562 12629456 Dyspnoea exertional
126294562 12629456 Headache
126294562 12629456 Hypersomnia
126294562 12629456 Incorrect dose administered
126294562 12629456 Lethargy
126294562 12629456 Oxygen saturation abnormal
126294562 12629456 Rhinorrhoea

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
126294562 12629456 2 20131210 0
126294562 12629456 3 20131210 0
126294562 12629456 4 20131210 0
126294562 12629456 5 20131210 0
126294562 12629456 6 20131210 0
126294562 12629456 7 20131210 0