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
124026872 12402687 2 F 20160512 20160816 20160525 20160824 PER US-ALEXION PHARMACEUTICALS INC-A201603620 ALEXION 32.99 YR M Y 0.00000 20160824 CN US US

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
124026872 12402687 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, Q2W 158400 MG U T2-AE4703B04 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW
124026872 12402687 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, Q2W 158400 MG U 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION QOW

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124026872 12402687 1 Paroxysmal nocturnal haemoglobinuria

Outcome of event

Event ID CASEID OUTC COD
124026872 12402687 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124026872 12402687 Fatigue
124026872 12402687 Haemolysis
124026872 12402687 Incorrect dose administered

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
124026872 12402687 1 20090626 20160503 0
124026872 12402687 2 20160816 0