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
126816671 12681667 1 I 20160811 20160824 20160824 PER US-ALEXION-A201605956 ALEXION 0.00 F Y 0.00000 20160824 PH 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
126816671 12681667 1 PS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 900 MG, QW N 125166 900 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk
126816671 12681667 2 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) UNK UNK, Q2W N 125166 CONCENTRATE FOR SOLUTION FOR INFUSION QOW
126816671 12681667 3 SS SOLIRIS ECULIZUMAB 1 Intravenous (not otherwise specified) 1200 MG, QW N 125166 1200 MG CONCENTRATE FOR SOLUTION FOR INFUSION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126816671 12681667 1 Haemolytic uraemic syndrome

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126816671 12681667 Inappropriate schedule of drug administration
126816671 12681667 Platelet count decreased

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
126816671 12681667 1 20160804 0
126816671 12681667 2 20160804 0