The Safety Rates Drug Report

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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
125542961 12554296 1 I 20160705 20160705 20160713 20160713 EXP GB-ALEXION PHARMACEUTICALS INC.-A201605147 ALEXION 74.80 YR M Y 0.00000 20160713 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
125542961 12554296 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 600 MG, QW P0004102 125166 600 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk
125542961 12554296 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 600 MG, QW P0004708 125166 600 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk
125542961 12554296 3 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, QW P0004801 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125542961 12554296 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
125542961 12554296 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125542961 12554296 Dyspnoea
125542961 12554296 Haemoglobin decreased
125542961 12554296 Inappropriate schedule of drug administration

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
125542961 12554296 1 20160614 20160705 0
125542961 12554296 2 20160614 20160705 0
125542961 12554296 3 20160705 0